Retardation material-forming resin composition, orientation material, and retardation material

ABSTRACT

A retardation material-forming resin composition for providing an orientation material that has high photoreaction efficiency and with which a polymerizable crystal can be aligned in a highly sensitive manner. A retardation material-forming resin composition being thermally curable wherein including a resin (component (A)) having a photo-aligning group to which a thermally reactive moiety is bonded directly or connected via a linking group; an orientation material obtained by use of the composition, and a retardation material formed by use of a cured film obtained from the composition.

This application is a divisional application of U.S. Pat. No. 15/122,277filed Aug. 29, 2016. which is in turn a U.S. National Stage ofInternational Application No. PCT/JP2015/055969, filed Feb. 27, 2015,which claims the benefit of Japanese Patent Application Nos. 2014-140946filed Jul. 8, 2014, and 2014-039699 filed Feb. 28, 2014, The disclosureof the prior applications is hereby incorporated by reference herein intheir entireties.

TECHNICAL HELD

The present invention relates to a retardation material-forming resincomposition, an orientation material, and a retardation material.

BACKGROUND ART

Recently, in the field of displays such as televisions including liquidcrystal panels, 3D displays with which 3D images can be enjoyed havebeen developed in order to enhance performance. In such 3D displays, astereoscopic image can be displayed by, for example, making the righteye of a viewer visually recognize an image for the right eye and makingthe left eye of the viewer visually recognize an image for the left eye.

Various 3D display methods for displaying 3D images can be used, andexamples of the methods known as methods requiring no special eyeglassesinclude a lenticular lens method and a parallax barrier method.

As one of display methods for viewers to see 3D images with eyeglasses,a circularly polarized glasses method, for example, is known (see PatentDocument 1, for example).

In a 3D display using the circularly polarized light glasses method, aretardation material is generally arranged on a display element forforming an image of a liquid crystal panel and the like. In thisretardation material, two types of retardation regions having differentretardation characteristics are regularly arranged each in plurality toconstitute a retardation material that is patterned. In the presentspecification, a retardation material thus patterned in which aplurality of retardation regions having different retardationcharacteristics are arranged is called a patterned retardation materialhereinafter.

The patterned retardation material can be fabricated by opticallypatterning a retardation substance including a polymerizable liquidcrystal as described in Patent Document 2, for example. In the opticalpatterning of the retardation substance including a polymerizable liquidcrystal, a photo-alignment technique known for forming an orientationmaterial for a liquid crystal panel is used. More specifically, acoating made of a material having photo-alignment properties is providedon a substrate, and two types of polarized beams the polarizationdirections of which are different from each other are radiated on thiscoating. Thus, a photo-alignment film is obtained as an orientationmaterial in which two types of liquid crystal alignment regions areformed and the directions of alignment control of liquid crystals in theregions are different from each other. Onto this photo-alignment film, aretardation substance containing a polymerizable liquid crystal in asolution state is applied to perform alignment of the polymerizableliquid crystal. Subsequently, the polymerizable liquid crystal thusaligned is cured to form a patterned retardation material.

As materials having photo-alignment properties that can be used inorientation material formation using a photo-alignment technique forliquid crystal panels, an acrylic resin and a polyimide resin, forexample, are known having in a side chain thereof a photodimerizedmoiety such as cinnamoyl group and chalcone group, for example. It isreported that these resins exhibit a property of controlling alignmentof liquid crystals (hereinafter, also called liquid crystal alignmentproperties) by polarized UV irradiation (see Patent Document 3 to PatentDocument 5).

PRIOR-ART DOCUMENTS Patent Documents

Patent Document 1: Japanese Patent Application Publication No. 10-232365(JP H10-232365 A)

Patent Document 2: Japanese Patent Application Publication No.2005-49865 (JP 2005049865 A)

Patent Document 3: Japanese Patent No. 3611342 (JP 3611342 B2)

Patent Document 4: Japanese Patent Application Publication No.2009-058584 (JP 2009-058584 A)

Patent Document 5: Published Japanese Translation of PCT Application No.2001-517719 (JP 2001-517719 A)

SUMMARY OF THE INVENTION Problem to be Solved by the Invention

However, according to the study by the inventors of the presentinvention, such acrylic resins having in a side chain thereof aphotodimerized moiety such as cinnamoyl group and chalcone group do notprovide sufficient properties when the acrylic resins are used forformation of a retardation material. In particular, to irradiate theseresins with polarized UV light to form an orientation material andoptically pattern a retardation substance including a polymerizableliquid crystal using the orientation material, a large exposure amountof polarized UV light is necessary. This makes the exposure amount ofthe polarized UV light much larger than the exposure amount (e.g., about30 mJ/cm²) of polarized UV light sufficient to align a liquid crystalfor a general liquid crystal panel.

A cause of the larger exposure amount of the polarized UV light is that,in formation of a retardation material, a polymerizable liquid crystalin a state of solution is used to be applied onto an orientationmaterial differently from the case of a liquid crystal for a liquidcrystal panel.

When an acrylic resin having in a side chain thereof a photodimerizedmoiety such as cinnamoyl group, for example, is used to form anorientation material, thereby aligning the polymerizable liquid crystal,in such an acrylic resin, photocrosslinking by photodimerizationreaction is performed. This requires irradiation with polarized light ina large exposure amount until the resistance to the polymerizable liquidcrystal solution appears. In order to align a liquid crystal of a liquidcrystal panel, only the surface of an orientation material withphoto-alignment properties generally needs to be subjected todimerization reaction. However, in order for an orientation material tohave solvent resistance when a conventional material such as the acrylicresin is used, the orientation material needs to be caused to react tothe inside thereof, which requires a larger exposure amount.Consequently, the alignment sensitivity of the conventional material issignificantly reduced disadvantageously.

A technique is known in which a cross-linking agent is added to theresin of the conventional material such that the resin has such solventresistance. However, it is known that a three-dimensional structure isformed inside a coating film that is formed after heat-curing reactionwith a cross-linking agent is performed, whereby the photoreactivity isreduced. In other words, the alignment sensitivity is significantlyreduced, and even if a conventional material to which the cross-linkingagent is added is used, a desired effect cannot be obtained.

In view of the foregoing, a photo-alignment technique that can improvethe alignment sensitivity of an orientation material to reduce theexposure amount of polarized UV light and a retardation material-formingresin composition that is used to form the orientation material aredesired. A technique is also desired that can efficiently provide apatterned retardation material.

The present invention has been made based on the above-describedfindings and study results. An object of the present invention is toprovide a retardation material-forming resin composition for providingan orientation material that has high photoreaction efficiency and withwhich a polymerizable liquid crystal can be aligned in a highlysensitive manner.

Another object of the present invention is to provide an orientationmaterial that is formed of the retardation material-forming resincomposition, has high photoreaction efficiency, and also has solventresistance and adhesion durability, and with which a polymerizableliquid crystal can be aligned in a highly sensitive manner, and toprovide a retardation material that is formed of the orientationmaterial.

The other objects and advantages of the present invention will beapparent from the following description.

Means for Solving the Problem

A first aspect of the present invention relates to a retardationmaterial-forming resin composition being thermally curable andcharacterized h comprising a resin [component (A)] having aphoto-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group.

In the first aspect of the present invention, the photo-aligning groupis preferably an organic group including a structure of Formula (1):

(in the Formula, R is a hydroxy group or an amino group, and X¹ is aphenylene group that is optionally substituted with an optionalsubstituent).

In the first aspect of the present invention, the resin of the component(A) is preferably an acrylic copolymer.

In the first aspect of the present invention, the resin of the component(A) preferably further has a self-crosslinking group, or further has agroup that reacts with at least one group A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2) [when an end portion ofthe photo-aligning group in the resin is carboxy group or amide group,this end portion is also included in the group A]:

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

In the first aspect of the present invention, the resin of the component(A) preferably further has at least one group A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2) [when an end portion ofthe photo-aligning group in the resin is carboxy group or amide group,this end portion is also included in the group A], and the compositionpreferably further includes a cross-linking agent (B) that reacts withthe at least one group A:

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

In the first aspect of the present invention, the resin of the component(A) preferably further has a group that reacts with at least one group Aselected from the group consisting of hydroxy group, carboxy group,amide, group, amino group, an alkoxysilyl group, and a group of Formula(2) [when an end portion of the photo-aligning group in the resin iscarboxy group or amide group, this end portion is also included in thegroup A], and the at least one group A:

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

In the first aspect of the present invention, the retardation materialforming resin composition preferably further comprises, as a component(C), a compound having at least two groups A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2).

In the first aspect of the present invention, the retardation materialforming resin composition preferably further comprises a cross-linkingcatalyst as a component (D).

In the first aspect of the present invention, the retardationmaterial-forming resin composition preferably further comprises, as acomponent (E): a compound having one or more polymerizable groups and atleast one group A selected from the group consisting of hydroxy group,carboxy group, amide group, amino group, an alkoxysilyl group, and agroup of Formula (2), or one or more groups that react with the at leastone croup A.

In the first aspect of the present invention, the retardationmaterial-forming resin composition preferably further comprises, as acomponent (F), a monomer having a photo-aligning group to which athermally reactive moiety is bonded directly or connected via a linkinggroup and one or more polymerizable groups.

A second aspect of the present invention relates to an orientationmaterial characterized by being obtained with the retardationmaterial-forming resin composition of the first aspect of the presentinvention.

A third aspect of the present invention relates to a retardationmaterial characterized by being formed with a cured film that isobtained from the retardation material-forming resin composition of thefirst aspect of the present invention.

A fourth aspect of the present invention relates to, a thermallycured-film formation composition characterized by comprising a resin[component (A)] having a photo-aligning group to which a thermallyreactive moiety is bonded directly or connected via a linking group.

In the fourth aspect of the present invention, the photo-aligning groupis preferably an organic group including a structure of Formula (1):

(in the Formula, R is a hydroxy group or an amino group; and X¹ is aphenylene group that is optionally substituted with an optionalsubstituent).

In the fourth aspect of the present invention, the resin of thecomponent (A) is preferably an acrylic copolymer.

In the fourth aspect of the present invention, the resin of thecomponent (A) preferably further has a self-crosslinking group, orfurther has a group that reacts with at least one group A selected fromthe group consisting of hydroxy group, carboxy group, amide group, aminogroup, an alkoxysilyl group, and a group of Formula (2) [when an endportion of the photo-aligning group in the resin is carboxy group oramide group, this end portion is also included in the group A]:

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

In the fourth aspect of the present invention, the resin of thecomponent (A) preferably further has at least one group A selected fromthe group consisting of hydroxy group, carboxy group, amide group, aminogroup, an alkoxysilyl group, and a group of Formula (2) [when an endportion of the photo-aligning group in the resin is carboxy group oramide group, this end portion is also included in the group A], and thecomposition preferably further includes a cross-linking agent (B) thatreacts with the at least one group A:

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

In the fourth aspect of the present invention, the resin of thecomponent (A) preferably further has a group that reacts with at leastone group A selected from the group consisting of hydroxy group, carboxygroup, amide group, amino group, an alkoxysilyl group, and a group ofFormula (2) [when an end portion of the photo-aligning group in theresin is carbon; group or amide group, this end portion is also includedin the group A], and the at least one group A:

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

In the fourth aspect of the present invention, the thermally cured-filmformation composition preferably further comprises, as a component (C),a compound having at least two groups A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2).

A fifth aspect of the present invention relates to a cured filmcharacterized by being obtained with the thermally cured-film formationcomposition of the fourth aspect of the present invention.

Effects of the Invention

According to the first aspect of the present invention, a retardationmaterial-forming resin composition that has excellent adhesion,alignment sensitivity, pattern formidability, and adhesion durabilityand can form an orientation material with which a polymerizable liquidcrystal can be aligned even on a resin film in a highly sensitive mannercan be provided.

According to the second aspect of the present invention, an orientationmaterial that has excellent adhesion, alignment sensitivity, patternformability, and adhesion durability, and with which a polymerizableliquid crystal can be aligned in a highly sensitive manner can beprovided.

According to the third aspect of the present invention, a retardationmaterial that can be efficiently formed and optically patterned even ona resin film can be provided.

According to the fourth aspect of the present invention, a thermallycured-film formation composition that can form a cured film having hightransparency, high solvent resistance, high heat resistance, and alsoliquid crystal alignment capability by light irradiation(photo-alignment properties) can be provided.

According to the fifth aspect of the present invention, a cured filmhaving high transparency, high solvent resistance, high heat resistance,and also liquid crystal alignment capability by light irradiation(photo-alignment properties) can be provided.

MODES FOR CARRYING OUT THE INVENTION

<Retardation Material-Forming Resin Composition>

A retardation material-forming resin composition of the presentinvention is used to form a thermally cured film having photo-alignmentproperties, and contains a component having a photo-alignment moiety anda moiety for thermal cross-linking. A photo-aligning group ischaracterized by being a specific photo-aligning group, that is, aphoto-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group.

As for the specific photo-aligning group, for example, when thephoto-aligning group is a cinnamic acid residue, the cinnamic acidresidue has carboxy group that is a thermally cross-linking group as apart of the residue. When a thermally cross-linking group forms a partof a photoreactive group in this manner also, the photoreactive groupcan be included in the specific photo-aligning group in the compositionof the present invention.

In the present invention, only any one component in the compositionneeds to have both of the group A and a group that reacts with the groupA as the moiety for thermal cross-linking, or only any one component inthe composition including a resin of a component (A) needs to have amoiety that self-crosslinks by heat. Thus, the retardationmaterial-forming resin composition of the present invention contains aresin having the specific photo-aligning group as the component (A),that is, a photo-aligning group to which a thermally reactive moiety isbonded directly or connected via a linking group, and further contains athermally cross-linking system.

As one aspect of the present invention, examples include a compositionthat contains the resin having the specific photo-aligning group as thecomponent (A) and, as a component (B), a cross-linking agent that reactswith the thermally reactive moiety connected to the specificphoto-aligning group. In this case, the resin of the component (A) onlyneeds to have, as a thermally reactive moiety, the thermally reactivemoiety in the specific photo-aligning group.

As one aspect of the present invention, examples include a compositionin which the resin of the component (A) is a copolymer with a monomerhaving the group A, and that contains, as the component (B), across-linking agent that thermally reacts with the group A.

As one aspect of the present invention, examples include a compositionthat further contains a self-crosslinking group as a thermallycross-linking system in the resin of the component (A).

As one aspect of the present invention, examples include a compositionthat further contains a group that reacts with a thermally reactivemoiety connected to the specific photo-aligning group, as the thermallycross-linking system in the resin of the component (A).

The retardation material-forming resin composition of the presentinvention may contain a cross-linking agent as the component (B) inaddition to the component (A). Furthermore, in addition to the component(A) and the component (B), the retardation material-forming resincomposition of the present invention may further contain: as a component(C), a compound having at least two groups A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2); a cross-linking catalystas a component (D); as a component (E), a compound having one or morepolymerizable groups and at least one group A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2), or one or more groupsthat react with the at least one group A; and as a component (F), amonomer having a photo-aligning group to which a thermally reactiveimpiety is bonded directly or connected via a linking group and one ormore polymerizable groups.

(In the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup.)

The retardation material-forming resin composition of the presentinvention may contain other additives as long as the effects of thepresent invention are not impaired.

Details of each component will be described below.

<Component (A)>

The component (A) contained in the retardation material-forming resincomposition of the present invention is a resin having a photo-aligninggroup to which a thermally reactive moiety is bonded directly orconnected via a linking group (hereinafter, also simply called“photo-aligning group”).

Examples of a structural moiety that the resin of the component (A) mayhave as a thermally reactive moiety include carboxy group, amide group,an N-substituted amide group, hydroxy group, amino group, an alkoxysilylgroup, and a group of Formula (2). Among them, the carboxy group and theamide group are preferred.

The photo-aligning group is a functional group of a structural moiety tobe photodimerized or photoisomerized.

The structural moiety to be photodimerized contained as thephoto-aligning group in the resin of the component (A) is a moiety thatforms a dimer by irradiation with light, and specific examples thereofinclude cinnamoyl group, chalcone group, coumarin group, and anthracenegroup. Among them, in terms of high transparency in the visible lightrange and high photodimerization reactivity, the cinnamoyl group ispreferred.

The structural moiety to be photoisomerized contained as thephoto-aligning group in the resin of the component (A) is a structuralmoiety that is converted into a cis form or a trans form by irradiationwith light, and specific examples thereof include a moiety containing anazobenzene structure and a moiety containing stilbene structure. Amongthem in terms of high reactivity, the azobenzene structure is preferred.

The thermally reactive moiety is bonded directly to or connected via alinking group to the photo-aligning group, and such a linking group is adivalent group selected from a linear alkylene group having a carbonatom number of 1 to 15, a branched alkylene group having a carbon atomnumber of 3 to 20, a cyclic alkylene group having a carbon atom numberof 3 to 20, and phenylene group, or a group formed by bonding together aplurality of such divalent groups. In this case, bonding between thedivalent groups forming the linking group and bonding between thelinking group and the thermally reactive moiety are achieved by a singlebond, an ester bond, an amide bond, a urea bond, or an ether bond. Whenthe divalent group is formed in plurality, the divalent groups may beidentical to or different from each other, and when such bonding isachieved by a plurality of bonds, the bonds may be identical to ordifferent from each other.

Examples of the linear alkylene group having a carbon atom number of 1to 15 include methylene group, ethylene group, n-propylene group,n-butylene group, n-pentylene group, n-hexylene group, n-heptylenegroup, n-octylene group, n-nonylene group, n-decylene group,n-undecylene group, n-dodecylene group, n-tridecylene group,n-tetradecylene group, and n-pentadecylene group.

Examples of the branched alkylene group having a carbon atom number of 3to 20 include i-propylene group, i-butylene group, s-butylene group,t-butylene group, 1-methyl-n-butylene group, 2-methyl-n-butylene group,3-methyl-n-butylene group, 1,1-dimethyl-n-propylene group,1,2-dimethyl-n-propylene group, 2,2-dimethyl-n-propylene group,1-ethyl-n-propylene group, 1-methyl-n-pentylene group,2-methyl-n-pentylene group, 3-methyl-n-pentylene group,4-methyl-n-pentylene group, 1,1-dimethyl-n-butylene group,1,2-dimethyl-n-butylene group, 1,3-dimethyl-n-butylene group,2,2-dimethyl-n-butylene group, 2,3-dimethyl-n-butylene group,3,3-dimethyl-n-butylene group, 1-ethyl-n-butylene group,2-ethyl-n-butylene group, 1,1,2-trimethyl-n-propylene group,1,2,2-trimethyl-n-propylene group, 1-ethyl-1-methyl-n-propylene group,and 1-ethyl-2-methyl-n-propylene group, and also an alkylene group thatis branched at an optional position within a range of up to C₂₀.

Examples of the cyclic alkylene group having a carbon atom number of 3to 20 include monocyclic alkylene groups such as cyclopropylene group,cyclobutylene group, cyclopentylene group, cyclohexylene group,cycloheptylene group, and cyclooctylene group; and polycyclic alkylenegroups such as norbornylene group, tricyclodecylene group,tetracyclododecylene group, and adamantylene group.

The resin of the component (A) is preferably an acrylic copolymer.

In the component (A), the photo-aligning group to which a thermallyreactive moiety is bonded directly or connected via a linking group ispreferably an organic group, for example, including a structure ofFormula (1):

(in the Formula, R is a hydroxy group, an amino group, a hydroxyphenoxygroup, a carboxyphenoxy group, an aminophenoxy group, an aminocarbonylphenoxy group, a phenylamino group, a hydroxy phenylamino group, acarboxy phenylamino group, an amino phenylamino group, a hydroxy alkylamino group, or a bis(hydroxyalkyl)amino group; and X¹ is a phenylenegroup that is optionally substituted with an optional substituent, inwhich a benzene ring in the definition of these substituents isoptionally substituted with a substituent).

Although the optional substituent is not limited to a particularsubstituent, examples thereof include alkyl groups such as methyl group,ethyl group, propyl group, butyl group, and isobutyl group; haloalkylgroups such as trifluoromethyl group; alkoxy groups such as methoxygroup and ethoxy group; halogen atoms such as iodine, bromine, chlorine,and fluorine; cyano group; and nitro group.

Examples of the substituent with which a benzene ring is optionallysubstituted include alkyl groups such as methyl group, ethyl group,propyl group, butyl group, and isobutyl group; haloalkyl groups such astrifluoromethyl group; alkoxy groups, such as methoxy group and ethoxygroup; halogen atoms such as iodine, bromine, chlorine, and fluorine;cyano group, and nitro group.

In the R, hydroxy group or amino group is preferred, and the hydroxygroup is particularly preferred.

The component (A) is preferably a resin in which the organic groupincluding the structure of Formula (1) binds to the main chain via aspacer. The spacer is a divalent group selected from a linear alkylenegroup with a carbon atom number of 1 to 15, a branched alkylene grouphaving a carbon atom number of 3 to 20, a cyclic alkylene group having acarbon atom number of 3 to 20, and phenylene group, or a group formed bybonding together a plurality of such divalent groups. In this case,bonding between the divalent groups forming the spacer, bonding betweenthe spacer and the polymerizable group, and bonding between the spacerand the group of Formula (1) are achieved by a single bond, an esterbond, an amide bond, a urea bond, or an ether bond. When the divalentgroup is formed in plurality, the divalent groups may be identical to ordifferent from each other, and when such bonding is achieved by aplurality of bonds, the bonds may be identical to or different from eachother.

Specific examples of each of the linear alkylene group having a carbonatom number of 1 to 15, the branched alkylene group having a carbon atomnumber of 3 to 20, and the cyclic alkylene group having a carbon atomnumber of 3 to 20 have been described (supra).

Among them, the component (A) is preferably a resin having aphoto-aligning group of Formula (1) in which R is a hydroxy group or anamino group and X¹ is a phenylene group that is optionally substitutedwith an optional substituent, and more preferably an acrylic copolymerhaving the photo-aligning group.

In the present invention, the acrylic copolymer is a polymer that isobtained by using a monomer having an unsaturated double bond such as anacrylic acid ester, a methacrylic acid ester, and styrene forhomopolymerization or copolymerization. Thus, in addition to the acryliccopolymer, an acrylic polymer is categorized in the “acrylic copolymer”in the present invention.

The acrylic copolymer having the photo-aligning group (hereinafter, alsocalled “specific copolymer”) only needs to be an acrylic copolymerhaving such a structure, and the skeleton of a polymer main chain, thetype of a side chain constituting the acrylic copolymer, for example,are not particularly limited.

The acrylic copolymer of the component (A) has a weight-averagemolecular weight of preferably 1,000 to 200,000, more preferably 2,000to 150,000, and further preferably 3,000 to 100,000. An excessively highweight-average molecular weight exceeding 200,000 may reduce thesolubility in solvent, so that the handling property may deteriorate,and an excessively low weight-average molecular weight below 1,000 maycause insufficient curing during heat curing, so that the solventresistance and the heat resistance may decrease. The weight-averagemolecular weight herein is a value obtained by gel permeationchromatography (GPC) using polystyrene as the standard sample. The samemethod is used hereinafter in the present specification.

As a method for synthesizing the acrylic copolymer having thephoto-aligning group of the component (A), a method of polymerizing amonomer having a photo-aligning group, which is a monomer having thephoto-aligning group of Formula (1), for example, is simple and easy

Examples of the monomer having the photo-aligning group of Formula (I)include 4-(6-methacryloxyhexyl-1-oxy)cinnamic acid,

-   4-(6-acryloxyhexyl-1-oxy)cinnamic acid,    4-(3-methacryloxypropyl-1-oxy)cinnamic acid,-   4-(6-methacryloxyhexyl-1-oxy)cinnamamide,    4-(6-acryloxyhexyl-1-oxy)cinnamamide,-   4-(3-methacryloxypropyl-1-oxy)cinnamamide,-   4-(4-(3-methacryloxypropyl-1-oxy)acryloxy)benzoic acid,

4-(4-(6-methacryloxyhexyl-1-oxy)benzoyloxy)cinnamic acid,

-   4-(6-methacryloxyhexyl-1-oxy)-N-(4-cyanophenyl)cinnamamide, and-   4-(6-methacryloxyhexyl-1-oxy)-N-bishydroxyethyl cinnamamide.

The component (A) contained in the retardation material-forming resincomposition of the present invention is preferably an acrylic copolymerthat, in addition to the photo-aligning group, further has aself-crosslinking group, or further has a group (hereinafter, alsocalled “cross-linking group”) that reacts with at least one group Aselected from the group consisting of hydroxy group, carboxy group,amide group, amino group, an alkoxysilyl group, and a group of Formula(2) [when an end portion of the photo-aligning group is carboxy group oramide group, this end portion is also included in the group A].

(In the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup.)

In Formula (2), preferable examples of the alkyl group of R₅ includeC₁₋₂₀ alkyl groups, and C₁₋₅ alkyl groups.

Examples of these alkyl groups include methyl group, ethyl group,n-propyl group, i-propyl group, n-butyl group, i-butyl group, s-butylgroup, t-butyl group, n-pentyl group, 1-methyl-n-butyl group,2-methyl-n-butyl group, 3-methyl-n-butyl group, 1,1-dimethyl-n-propylgroup,2-dimethyl-n-propyl group, 2,2-dimethyl-n-propyl group,1-ethyl-n-propyl group, n-hexyl group, 1-methyl-n-pentyl group,2-methyl-n-pentyl group, 3-methyl-n-pentyl group, 4-methyl-n-pentylgroup, 1,1-dimethyl-n-butyl group, 1,2-dimethyl-n-butyl group,1,3-dimethyl-n-butyl group, 2,2-dimethyl-n-butyl group,2,3-dimethyl-n-butyl group, 3,3-dimethyl-n-butyl group, 1-ethyl-n-butylgroup, 2-ethyl-n-butyl group, 1,1,2-trimethyl-n-propyl group,1,2,2-trimethyl-n-propyl group, 1-ethyl-1-methyl-n-propyl group,1-ethyl-2-methyl-n-propyl group, n-heptyl group, n-octyl group, n-nonylgroup, n-decanyl group, n-undecyl group, n-dodecyl group, n-tridecylgroup, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group,n-heptadecyl group, n-octadecyl group, n-nonadecyl group, n-eicosylgroup, cyclopropyl group, cyclobutyl group, cyclopentyl group,cyclohexyl group, and cycloheptyl group.

Among them, methyl group, ethyl group, n-propyl group, n-butyl group,and isobutyl group, and the like are preferred.

In Formula (2), preferable examples of the alkoxy group of R₅ includeC₁₋₂₀ alkoxy groups, and C₁₋₅ alkoxy groups.

Examples of these alkoxy groups include methoxy group, ethoxy group,n-propoxy group, i-propoxy group, n-butoxy group, i-butoxy group,s-butoxy group, t-butoxy group, n-pentoxy group, 1-methyl-n-butoxygroup, 2-methyl-n-butoxy group, 3-methyl-n-butoxy group,1,1-dimethyl-n-propoxy group, 1,2-dimethyl-n-propoxy group,2,2-dimethyl-n-propoxy group, 1-ethyl-n-propoxy group, n-hexyloxy group,1-methyl-n-pentyloxy group, 2-methyl-n-pentyloxy group,3-methyl-n-pentyloxy group, 4-methyl-n-pentyloxy group, 1,1-dimethyl-n-butoxy group, 1, 2-dimethyl-n-butoxy group, 1,3-dimethyl-n-butoxy group, 2, 2-dimethyl-n-butoxy group, 2,3-dimethyl-n-butoxy group, 3, 3-dimethyl-n-butoxy group,1-ethyl-n-butoxy group, 2-ethyl-n-butoxy group, 1, 1,2-trimethyl-n-propoxy group, 1, 2, 2-trimethyl-n-propoxy group,1-ethyl-1-methyl-n-propoxy group, 1-ethyl-2-methyl-n-propoxy group,n-heptyloxy group, n-octyloxy group, n-nonyloxy group, n-decyloxy group,n-undecyloxy group, n-dodecyloxy group, n-tridecyloxy group,n-tetradecyloxy group, n-pentadecyloxy group, n-hexadecyloxy group,n-heptadecyloxy group, n-octadecyloxy group, n-nonadecyloxy group,n-eicosadecyloxy group, cyclopropoxy group, cyclobutoxy group,cyclopentyloxy group, cyclohexyloxy group, and cycloheptyloxy group.

Among them, the methoxy group, the ethoxy group, and the n-propoxygroup, and the like are preferred.

As a method for synthesizing the acrylic copolymer that further has aself-crosslinking group or further has a cross-linking group in additionto the photo-aligning group, a method of polymerizing a monomer havingthe photo-aligning group with a monomer having a self-crosslinking groupor a monomer having a cross-linking group is simple and easy.

Examples of the self-crosslinking group and the cross-linking groupinclude an alkoxymethylamide group, hydroxymethylamide group, analkoxysilyl group, glycidyl group, epoxycyclohexyl group, vinyl group,and a blocked isocyanate group. The content of the self-crosslinkinggroup or the cross-linking group to, be contained in the resin of thecomponent (A) is preferably 0.1 to 0.9 per repeating unit in the resinof the component (A), and more preferably 0.1 to 0.8 from the viewpointof balance between alignment properties and solvent resistance of theorientation material.

Examples of the monomer having a self-crosslinking group and across-linking group include a (meth)acrylamide compound substituted witha hydroxymethyl group or a alkoxymethyl group such asN-hydroxymethyl(meth) acrylamide, N-methoxymethyl(meth) acrylamide,N-ethoxymethyl(meth) acrylamide, and N-butoxymethyl(meth) acrylamide; amonomer having a trialkoxysilyl group such as 3-trimethoxysilylpropylacrylate, 3-triethoxysilyl propylacrylate, 3-trimethoxysilylpropylmethacrylate, and 3-triethoxysilylpropyl methacrylate; a monomer havingglycidyl group or epoxycyclohexyl group such as glycidyl acrylate,glycidyl methacrylate, and 3,4-epoxycyclohexlmethylmethacrylate; amonomer having a vinyl group such as 1,2-epoxy-5-hexene and1,7-octadiene monoepoxide; and a monomer having a blocked isocyanategroup such as 2(0-(1′-methylpropylideneamino)carboxyamino)ethylmethacrylate and 2-(3,5-dimethylpyrazolyl)carbonylamino)ethylmethacrylate. Herein, the (meth)acrylamide means both of acrylamide andmethacrylamide.

The component (A) contained in the retardation material-forming resincomposition of the present invention is preferably an acrylic copolymerthat further has, in addition to the photo-aligning group, at least onegroup A selected from the group consisting of hydroxy group, carboxygroup, amide group, amino group, an alkoxysilyl group, and a group ofFormula (2) [when an end portion of the photo-aligning group is carboxygroup or amide group, this end portion is also included in the group A].

Examples of the group of Formula (2) include structures:

As a method for synthesizing the acrylic copolymer that further has, inaddition to the photo-aligning group, at least one group A selected fromthe group consisting of hydroxy group, carboxy group, amide group, aminogroup, an alkoxysilyl group, and a group of Formula (2), a method ofpolymerizing a monomer having the photo-aligning group with a monomerhaving the at least one group A selected from the group consisting ofhydroxy group, carboxy group, amide group, amino group, an alkoxysilylgroup, and a group of Formula (2) is simple and easy.

Examples of the monomer having at least one group A selected from thegroup consisting of hydroxy group, carboxy group, amide group, aminogroup, an alkoxysilyl group, and a group of Formula (2) include: amonomer having hydroxy group such as 2-hydroxyethyl acrylate,2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropylmethacrylate, 4-hydroxybutyl acrylate, 4-hydroxybutyl methacrylate,2,3-dihydroxypropyl acrylate, 2,3-dihydroxypropyl methacrylate,diethylene glycol monoacrylate, diethylene glycol monomethacrylate,caprolactone 2-(acryloyloxy)ethyl ester, caprolactone2-(methacryloyloxy)ethyl ester, poly(ethylene glycol)ethyletheracrylates, poly(ethylene glycol)ethylether methacrylates,5-acryloyloxy-6-hydroxynorbornene-2-carboxylic-6-lactone, and5-methacryloyloxy-6-hydroxynorbornene-2-carboxylic-6-lactone; a monomerhaving carboxy group such as acrylic acid, methacrylic acid, crotonicacid, mono-(2-(acryloyloxy)ethyl)phthalate,mono-(2-(methacryloyloxy)ethyl)phthalate, N-(carboxyphenyl)maleimide,N-(carboxyphenyl)methacrylamide, and N-(carboxyphenyl)acrylamide; amonomer having phenolic hydroxy group such as hydroxystyrene,N-(hydroxyphenyl)methacrylamide, N-(hydroxyphenyl)acrylamide,N-(hydroxyphenyl)maleimide, and N-(hydroxyphenyl)maleimide; a monomerhaving amide group such as acrylamide, methacrylamide,N-methylacrylamide, N,N-dimethylactylamide, and N,N-diethylacrylamide; amonomer having amino group such as aminoethyl acrylate, aminoethylmethacrylate, aminopropyl acrylate, and aminopropyl methacrylate; amonomer having an alkoxysilyl group such as 3-acryloyloxytrimethoxysilane, 3-acryloyloxy triethoxysilane, 3-methacryloyloxytrimethoxysilane, and 3-methacryloyloxy triethoxysilane and a monomerhaving a group of Formula (2) such as 2-acetoacetoxyethyl acrylate and2-acetoacetoxyethyl methacrylate (ethylene glycol mono-acetoacetatemonomethacrylate).

The component (A) contained in the retardation material-forming resincomposition of the present invention is preferably an acrylic copolymerthat further has, in addition to the photo-aligning group, a group(cross-linking group) that reacts with at least one group A selectedfrom the group consisting of hydroxy group, carboxy group, amide group,amino group, an alkoxysilyl group, and a group of Formula (2) [when anend portion of the photo-aligning group is carboxy group or amide group,this end portion is also included in the group A] and the at least onegroup A.

As a method for synthesizing the acrylic copolymer that further has, inaddition to the photo-aligning group, a cross-linking, group and atleast one group A selected from the group consisting of hydroxy group,carboxy group, amide group, amino group, an alkoxysilyl group, and agroup of Formula (2), a method of polymerizing a monomer having thephoto-aligning group with a monomer having a cross-linking group andalso with a monomer having at least one group A selected from the groupconsisting of hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2) is simple and easy.

The monomer having the photo-aligning group, the monomer having across-linking group, and the monomer having at least one group Aselected from the group consisting of hydroxy group, carboxy group,amide group, amino group, an alkoxysilyl group, and a group of Formula(2) have been described in the foregoing.

In the present invention, when the specific copolymer is obtained, inaddition to the monomer having the photo-aligning group, the monomerhaving a self-crosslinking group or the monomer having a cross-linkinggroup, and the monomer having at least one group A selected from hydroxygroup, carboxy group, amide group, amino group, an alkoxysilyl group,and a group of Formula (2) (hereinafter, the photo-aligning group, theself-crosslinking group, the cross-linking group, and the hydroxy group,the carboxy group, the amide group, the amino group, the alkoxysilylgroup, and the group of Formula (2) are called “specific functionalgroup 1”), another monomer that can be copolymerized with these monomersand does not have the specific functional group 1 can be used.

Specific examples of such another monomer include an acrylic acid estercompound, a methacrylic acid ester compound, a maleimide compound, anacrylamide compound, acrylonitrile, maleic anhydride, a styrenecompound, and a vinyl compound.

Specific examples of the monomer are described below, but the monomer isnot limited to these.

Examples of the acrylic acid ester compound include methyl acrylate,ethyl acrylate, isopropyl acrylate, benzyl acrylate, naphthyl acrylate,anthryl acrylate, anthrylmethyl acrylate, phenyl acrylate,2,2,2-trifluoroethyl acrylate, tert-butyl acrylate, cyclohexyl acrylate,isobornyl acrylate, 2-methoxyethyl acrylate, methoxytriethylene glycolacrylate, 2-ethoxyethyl acrylate, tetrahydrofurfuryl acrylate,3-methoxybutyl acrylate, 2-methyl-2-adamanthyl acrylate,2-propyl-2-adamanthyl acrylate, 8-methyl-8-tricyclodecyl acrylate, and8-ethyl-8-tricyclodecyl acrylate.

Examples of the methacrylic acid ester compound include methylmethacrylate, ethyl methacrylate, isopropyl methacrylate, benzylmethacrylate, naphthyl methacrylate, anthryl methacrylate, anthrylmethylmethacrylate, phenyl methacrylate, 2,2,2-trifluoroethyl methacrylate,tert-butyl methacrylate, cyclohexyl methacrylate, isobornylmethacrylate, 2-methoxyethyl methacrylate, methoxy triethylene glycolmethacrylate, 2-ethoxy ethyl methacrylate, tetrahydrofurfurylmethacrylate, 3-methoxybutyl methacrylate, 2-methyl-2-adamanthylmethacrylate, γ-butyrolactone methacrylate, 2-propyl-2-adamanthylmethacrylate, 8-methyl-8-tricyclodecyl methacrylate, and8-ethyl-8-tricyclodecyl methacrylate.

Examples of the vinyl compound include methylvinyl ether, benzylvinylether, vinyl naphthalene, vinyl carbazole, allyl glycidyl ether, and3-ethenyl-7-oxabicyclo[4.1.0]heptane

Examples of the styrene compound include styrene, methylstyrene,chlorostyrene, and bromostyrene.

Examples of the maleimide compound include maleimide, N-methylmaleimide,N-phenylmaleimide and N-cyclohexylmaleimide.

The amounts of the respective monomers to be used to obtain the specificcopolymer are, based on the total amount of all monomers, preferably 10%to 90% by mole for the monomer having the photo-aligning group, and 10%to 90% by mole for a monomer having a substituent selected from theself-crosslinking group, the group A, and the cross-linking group (theseare called “specific cross-linking group 1” as a whole, which includes asubstituent at an end of the photo-aligning group.). When the content ofthe monomer having the specific cross-linking group 1 is lower than 10%by mole, it is difficult to impart satisfactory thermosettingproperties, and it is also difficult to maintain highly sensitive andexcellent liquid crystal alignment properties.

When the monomer that does not have the specific functional group 1 isused to obtain the specific copolymer, the amount used of this monomeris preferably equal to or lower than 90% by mole, based on the totalamount of all monomers.

Although the method for obtaining the specific copolymer to be used inthe present invention is not limited to a particular method, thespecific copolymer can be obtained, for example, by subjecting themonomer having the specific functional group 1, a monomer that does nothave the specific functional group 1 if desired, and a polymerizationinitiator or the like to polymerization reaction in a solvent in whichthey coexist at a temperature of 50° C. to 110° C. The solvent to beused herein is not limited as long as the solvent can dissolve themonomer having the specific functional group 1, the monomer that doesnot have the specific functional group 1 used if desired, and apolymerization initiator or the like. Specific examples thereof will begiven in <Solvent> described below.

The specific copolymer to be obtained by the above-described method isgenerally in a solution state of being dissolved in the solvent.

A solution of the specific copolymer obtained by the method is pouredinto diethyl ether, water, or the like with stirring and the specificcopolymer is reprecipitated. The precipitate thus obtained is filteredand washed, and then is dried at room temperature or dried by heatingunder atmospheric pressure or reduced pressure. Thus, a powder of thespecific copolymer can be prepared. By this operation, thepolymerization initiator and an unreacted monomer that coexist with thespecific copolymer can be removed, and consequently, a powder of thepurified specific copolymer can be obtained. If the specific copolymercannot be sufficiently purified by one operation, the obtained powdermay be redissolved in a solvent, followed by repeating theabove-described operation.

In the present invention, the specific copolymer may be used in a formof powder or in a form of solution in which the purified powder isredissolved in a solvent described below.

In the present invention, the specific copolymer of the component (A)may be a mixture of a plurality of types of specific copolymers.

<Component (B)>

The retardation material-forming resin composition of the presentinvention may contain a crosslinking agent as the component (B).Examples of the component (B) include a cross-linking agent that reactswith at least one group A selected from the group consisting of hydroxygroup, carboxy group, amide group, amino group, an alkoxysilyl group,and a group of Formula (2).

Examples of the cross-linking agent that is the component (B) includecompounds such as an epoxy compound, a methylol compound, an isocyanatecompound, a phenoplast compound, a compound having two or moretrialkoxysilyl groups, and an alkoxysilane compound having amino group;an organometallic compound having an alkoxy group and/or a chelatingligand; and polymers such as a polymer of an N-alkoxymethyl acrylamide,a polymer of a compound having epoxy group, a polymer of a compoundhaving an alkoxysilyl group, a polymer of a compound having isocyanategroup, and a melamine formaldehyde resin.

Specific examples of the epoxy compound include ethyleneglycoldiglycidylether, polyethyleneglycol diglycidylether, propyleneglycoldiglycidylether, tripropyleneglycol diglycidylether, polypropyleneglycoldiglycidylether, neopentylglycol diglycidylether, 1,6-hexanedioldiglycidylether, glycerindiglycidylether,2,2-dibromoneopentylglycoldiglycidylether,1,3,5,6-tetraglycidyl-2,4-hexanediol,N,N,N′,N′-tetraglycidyl-m-xylenediamine,1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, andN,N,N′,N′-tetraglycidyl-4,4′-diaminodiphenylmethane.

Specific examples of the methylol compound include compounds such as analkoxymethylated glycoluril, an alkoxymethylated benzoguanamine, and analkoxymethylated melamine.

Specific examples of the alkoxymethylated glycoluril include1,3,4,6-tetrakis(methoxymethyl)glycoluril,1,3,4,6-tetrakis(butoxymethyl)glycoluril,1,3,4,6-tetrakis(hydroxymethyl)glycoluril, 1,3-bis(hydroxymethyl)urea,1,1,3,3-tetrakis(butoxymethyl)urea, 1,1,3,3-tetrakis(methoxymethyl)urea,1,3-bis(hydroxymethyl)-4,5-dihydroxy-2-imidazolinone, and1,3-bis(methoxymethyl)-4,5-dimethoxy-2-imidazolino. Examples ofcommercially available products thereof include: compounds such asglycoluril compounds (trade name: CYMEL (registered trademark) 1170, andPowderlink (registered trademark) 1174), methylated urea resins (tradename: UFR (registered trademark) 65), and butylated urea resins (tradename: UFR (registered trademark) 300, U-VAN10S60, U-VAN10R, andU-VAN11HV) manufactured by Mitsui Cytec Ltd.; andurea/formaldehyde-based resins (highly condensed type, trade name:Beckamine (registered trademark) J-300S, Beckamine P-955, and BeckamineN) manufactured by DIC Corporation.

Specific examples of the alkoxymethylated benzoguanamine includetetramethoxymethyl benzoguanamine. Examples of commercially availableproducts thereof include a product (trade name: CYMEL (registeredtrademark) 1123) manufactured by Mitsui Cytec Ltd. and products (tradename: NIKALAC (registered trademark) BX-4000, NIKALAC BX-37, NIKALACBL-60, and NIKALAC BX-55H) manufactured by Sanwa Chemical Co., Ltd.

Specific examples of the alkoxymethylated melamine includehexamethoxymethyl melamine. Examples of commercially available productsthereof include methoxymethyl-type melamine compounds (trade name: CYMEL(registered trademark) 300, CYMEL 301, CYMEL 303 and CYMEL 350) andbutoxymethyl-type melamine compounds (trade name: Mycoat (registeredtrademark) 506, and 508) manufactured by Mitsui Cytec Ltd., andmethoxymethyl-type melamine compounds (trade name: NIKALAC (registeredtrademark) MW-30, NIKALAC MW-22, NIKALAC MW-11 NIKALAC MS-001 NIKALACMX-002, NIKALAC MX-730, NIKALAC MX-750, and NIKALAC MX-035) andbutoxymethyl-type melamine compounds (trade name: NIKALAC (registeredtrademark) MX-45, NIKALAC MX-410, and NIKALAC MX-302) manufactured bySanwa Chemical Co., Ltd.

The component (B) may also be a compound to be obtained by condensing amelamine compound, a urea compound, a glycoluril compound, or abenzoguanamine compound in which a hydrogen atom of amino group issubstituted with methylol group or an alkoxymethyl group. Examplesthereof include a high-molecular-weight compound produced from amelamine compound or a benzoguanamine compound described in U.S. Pat.No. 6,323,310. Examples of commercially available products of themelamine compound include a product trade-named CYMEL (registeredtrademark) 303 (manufactured by Mitsui Cytec Ltd.), and examples ofcommercially available products of the benzoguanamine compound include aproduct trade-named CYMEL (registered trademark) 1123 (manufactured byMitsui Cytec Ltd.).

Specific examples of the isocyanate compound include VESTANAT B1358/100and VESTAGON BF 1540 (these are isocyanurate-type modifiedpolyisocyanates manufactured by Degussa Japan Co., Ltd.), and Takenate(registered trademark) B-882N and Takenate 13-7075 (these areisocyanurate-type modified polyisocyanates manufactured by MitsuiChemicals, Inc.).

Specific examples of the phenoplast compound include compounds below,but the phenoplast compound is not limited to these exemplifiedcompounds.

Specific examples of the compound having two or more trialkoxysilylgroups include compounds such as 1,4-bis(trimethoxysilyl)benzene,1,4-bis(triethoxysilyl)benzene, 4,4′-bis(trimethoxysilyl)biphenyl,4,4′-bis(triethoxysilyl)biphenyl, bis(trimethoxysilyl)ethane,bis(triethoxysilyl)ethane, bis(trimethoxysilyl)methane,bis(triethoxysilyl)methane, bis(trimethoxysilyl)ethylene,bis(triethoxysilyl)ethylene,1,3-bis(trimethoxysilylethyl)tetramethyldisiloxane,1,3-bis(triethoxysilylethyl)tetramethyldisiloxane, bis(triethoxysilylmethyl)amine, bis(trimethoxysilyl methyl)amine,bis(triethoxysilylpropyl)amine, bis(trimethoxysilylpropyl)amine,bis(3-trimethoxysilyl propyl)carbonate, bis(3-triethoxysilylpropyl)carbonate, bis[(3-trimethoxysilyl)propyl]disulfide,bis[(3-triethoxysilyl)propyl]disulfide,bis[(3-trimethoxysilyl)propyl]thiourea,bis[(3-triethoxysilyl)propyl]thiourea,bis[(3-trimethoxysilyl)propyl]urea, bis[(3-triethoxysilyl)propyl]urea,4-bis(trimethoxysilylmethyl)benzene,1,4-bis(triethoxysilylmethyl)benzene, tris(trimethoxysilylpropyl)amine,tris(triethoxysilylpropyl)amine, 1,1,2-tris(trimethoxysilyl)ethane,1,1,2-tris(triethoxysilyl)ethane,tris(3-trimethoxysilylpropyl)isocyanurate, andtris(3-triethoxysilylpropyl)isocyanurate.

Specific examples of the alkoxysilane compound having amino groupinclude compounds such asN,N′-bis[3-(trimethoxysilyl)propyl]-1,2-ethanediamine,

-   N,N′-bis[3-(triethoxysilyl)propyl]-1,2-ethanediamine,-   N-[3-(trimethoxysilyl)propyl]-1,2-ethanediamine,-   N-[3-(triethoxysilyl)propyl]-1,2-ethanediamine,    bis-{3-(trimethoxysilyl)propyl}amine,-   bis-{3-(triethoxysilyl)propyl}amine, 3-aminopropyltrimethoxysilane,-   3-aminopropyltriethoxysilane,    trimethoxy{3-(methylamino)propylsilane,-   3-(N-allylamino)propyltrimethoxysilane,    3-(N-allylamino)propyltriethoxysilane,-   3-(diethylamino)propyltrimethoxysilane,    3-(diethylamino)propyltriethoxysilane,-   3-(phenylamino)propyltrimethoxysilane, and    3-(phenylamino)propyltriethoxysilane.

Specific examples of the organometallic compound having an alkoxy groupand/or a chelating ligand include compounds such as diisopropoxyethylacetoacetate aluminum, diisopropoxy acetylacetonate aluminum,triacetyl acetonate aluminum, tetrakis isopropoxy titanium, tetrakisn-butoxy titanium, tetraoctyl titanatediisopropoxybis(acetylacetonate)titanium, titanium tetraacetylacetonate,tetrakis(n-propoxy)zirconium, tetrakis(n-butoxy)zirconium, andtetrakis(acetylacetonate)zirconium.

Examples of the polymer of N-alkoxymethyl acrylamides include a polymerproduced by using an acrylamide compound or a methacrylamide compoundsubstituted with hydroxymethyl group or an alkoxymethyl group such asN-hydroxymethyl(meth)acrylamide, N-methoxymethyl(meth)acrylamide,N-ethoxymethyl(meth)acrylamide, and N-butoxymethyl(meth)acrylamide.

Specific examples of this polymer include apoly(N-butoxymethylacrylamide), a copolymer of N-butoxymethylacrylamidewith styrene, a copolymer of N-hydroxymethylmethacrylamide with methylmethacrylate, a copolymer of N-ethoxymethylmethacrylamide with benzylmethacrylate, and a copolymer of N-butoxymethylacrylamide andbenzylmethacrylate with 2-hydroxypropyl methacrylate. The weight-averagemolecular weight of the polymer is 1,000 to 200,000, more preferably3,000 to 150,000, and further preferably 3,000 to 50,000.

Examples of the polymer of a compound having epoxy group include apolymer produced by using a compound having epoxy group such as glycidylmethacrylate, 3,4-epoxycyclohexylmethyl methacrylate, and3,4-epoxycyclohexylmethyl methacrylate.

Specific examples of this polymer include apoly(3,4-epoxycyclohexylmethyl methacrylate), a poly(glycidylmethacrylate), a copolymer of glycidyl methacrylate with methylmethacrylate, a copolymer of 3, 4-epoxycyclohexylmethyl methacrylatewith methyl methacrylate, and a copolymer of glycidyl methacrylate withstyrene. The weight-average molecular weight of the polymer is 1,000 to200,000, more preferably 3,000 to 150,000, and further preferably 3,000to 50,000.

Examples of the polymer of a compound having an alkoxysilyl groupinclude a polymer produced by using a compound having an alkoxysilylgroup such as 3-methacryloxypropyl trimethoxysilane.

Specific examples of this polymer include a poly(3-methacryloxypropyltrimethoxy silane), a copolymer of 3-methacryloxypropyl trimethoxysilane with styrene, and a copolymer of 3-methacryloxypropyltrimethoxysilane with methyl methacrylate. The weight-average molecularweight of the polymer is 1,000 to 200,000, more preferably 3,000 to150,000, and further preferably 3,000 to 50,000. In the presentspecification, the “poly((meth)acryloxypropyltrimethoxy silane)” means apoly(meth)acrylate having an alkoxysilyl group.

Examples of the polymer of a compound having isocyanate group include apolymer produced by using a compound having isocyanate group such as2-isocyanatoethyl methacrylate (Karenz MOI [registered trademark]manufactured by Showa Denko K.K.) and 2-isocyanatoethyl acrylate (KarenzAOI [registered trademark] manufactured by Showa Denko K.K.), or acompound having a blocked isocyanate group such as2-(0-[1′-methylpropylideneamino]carboxyamino)ethyl methacrylate (KarenzMOI-BM [registered trademark] manufactured by Showa Denko K.K.) and2-[(3,5-dimethylpyrazolyl)carbonylamino]ethyl methacrylate (KarenzMOI-BP [registered trademark] manufactured by Showa Denko K.K.).

Specific examples of this polymer include a poly(2-isocyanatoethylacrylate), a poly(2-(0-[1′-methylpropylideneamino]carboxyamino)ethylmethacrylate), a copolymer of 2-isocyanatoethyl methacrylate withstyrene, and a copolymer of2-[(3,5-dimethylpyrazolyl)carbonylamino]ethyl methacrylate with methylmethacrylate. The weight-average molecular weight of the polymer is1,000 to 200,000, more preferably 3,000 to 150,000, and furtherpreferably 3,000 to 50,000.

The melamine formaldehyde resin described above is a resin that isobtained by polycondensation between melamine and formaldehyde, and is aresin of Formula:

(In the Formula, R²¹ is a hydrogen atom or a C₁₋₄ alkyl group; and n isa natural number representing the number of repeating units.)

In the melamine formaldehyde resin of the component (B), methylol groupgenerated in the polycondensation between melamine and formaldehyde ispreferably alkylated from the viewpoint of preservation stability.

Although the method for obtaining the melamine formaldehyde resin of thecomponent (B) is not limited to a particular method, the melamineformaldehyde resin is synthesized generally by mixing melamine andformaldehyde, making this mixture weakly alkaline with sodium carbonate,ammonia, or the like, and then heating the mixture at 60° C. to 100° C.By additional reaction with alcohol, the methylol group can bealkoxylated.

The melamine formaldehyde resin of the component (B) has aweight-average molecular weight of preferably 250 to 5,000, morepreferably 300 to 4,000, and further preferably 350 to 3,500. Anexcessively high weight-average molecular weight exceeding 5,000 mayreduce the solubility in solvent, so that the handling property maydeteriorate, and an excessively low weight-average molecular weightbelow 250 may cause insufficient curing during heat curing, so that theeffect of improving the solvent resistance and the heat resistancecannot be sufficiently obtained in some cases.

In the retardation material-forming resin composition of the presentinvention, the melamine formaldehyde resin of the component (B) may beused in a form of liquid or in a form of solution in which the purifiedliquid is redissolved in a solvent described below.

These cross-linking agents may be used singly or in combination of twoor more of them.

The content of the cross-linking agent of the component (B) in theretardation material-forming resin composition of the present inventionis preferably 0 part by mass to 100 parts by mass, and more preferably 0part by mass to 80 parts by mass, based on 100 parts by mass of thetotal amount of the resin of the component (A) and, as optionalcomponents, the component (C), the component (E), and the component (F).When the content of the cross-linking, agent is excessively high, thephoto-alignment properties and the preservation stability maydeteriorate.

<Component (C)>

The retardation material-forming resin composition of the presentinvention may contain, as the component (C), a compound having at leasttwo groups A (hereinafter, also called “specific functional group 2”)selected from the group consisting of hydroxy group, carboxy group,amide group, amino group, an alkoxysilyl group, and a group of Formula(2). The component (C) may be a low-molecular compound or may be ahigh-molecular compound.

Examples of the low-molecular compound that is the component (C) includepentaerythritol, dipentaerythritol, diethylene glycol, methylene glycol,dipropylene glycol, adipic acid, adipamide, hexamethylenediamine,1,4-bis(acetoacetyl aminoethyl)cyclohexane,1-(4-(2-(4-(3-oxo-butyl)-phenoxy)-ethoxy)-phenyl)-butane-1,3-dione, and1,4-butanediol diacetoacetate.

Examples of the high-molecular compound that is the component (C)include a polymer having a straight-chain structure or a branchedstructure such as an acrylic polymer, a polyamic acid, a polyimide, apolyvinyl alcohol, a polyester, a polyester polycarboxylic acid, apolyester polyol, a polyester polyol, a polycarbonate polyol, apolycaprolactone polyol, a polyalkylene imine, a polyallylamine,celluloses (cellulose or derivatives thereof), and a phenol novolacresin; and a cyclic polymer such as cyclodextrins.

Preferred examples of the high-molecular compound that is the component(C) include an acrylic polymer, cyclodextrins, celluloses, a polyetherpolyol, a polyester polyol, a polycarbonate polyol, a polycaprolactonepolyol and a phenol novolac resin.

The acrylic polymer that is one preferred example of the high-molecularcompound of the component (C) is a polymer that is obtained bypolymerizing a monomer having an unsaturated double bond such as acrylicacid, methacrylic acid, styrene, and a vinyl compound, and only needs tobe a polymer that is obtained by polymerizing monomers containing thegroups A or a mixture thereof. The skeleton of a polymer main chain andthe type of a side chain constituting the acrylic polymer, for example,are not particularly limited.

Examples of the monomers containing the groups A include a monomerhaving a polyethylene glycol ester group, a monomer having a C₂₋₅hydroxyalkyl ester group, a monomer having a phenolic hydroxy group, amonomer having carboxy group, a monomer having amide group, a monomerhaving amino group, and a monomer having a group of Formula (2).

Examples of the monomer having a polyethylene glycol ester group includemonoacrylate or monomethacrylate of H—(OCH₂CH₂)n-OH. Herein, the valueof n is 2 to 50, and preferably 2 to 10.

Examples of the monomer having a C₂₋₅ hydroxyalkyl ester group include2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropylmethacrylate, 2-hydroxypropyl acrylate, 4-hydroxybutyl acrylate, and4-hydroxybutyl methacrylate.

Examples of the monomer having a phenolic hydroxy group includep-hydroxystyrene, m-hydroxystyrene, and o-hydroxystyrene.

Examples of the monomer having carboxy group include acrylic acid,methacrylic acid, and vinylbenzoic acid.

Examples of the monomer having amide group include acrylamide andmethacrylamide.

Examples of the monomer having amino group include 2-aminoethylacrylate, 2-aminoethyl methacrylate, aminopropyl acrylate, andaminopropyl methacrylate.

Examples of the monomer having an alkoxysilyl group include3-acryloyloxy trimethoxysilane, 3-acryloyloxy triethoxysilane,3-methacryloyloxy trimethoxysilane, and 3-methacryloyloxytriethoxysilane.

Examples of the monomer having a group of Formula (2) include2-acetoacetoxyethyl acrylate and 2-acetoacetoxyethyl methacrylate.

When the acrylic polymer that is an example of the component (C) issynthesized in the present invention, a monomer that does not have thespecific functional group 2 may be used as long as the effects of thepresent invention are not impaired.

Specific examples of this monomer include an acrylic acid estercompound, a methacrylic acid ester compound, a maleimide compound,acrylonitrile, maleic anhydride, a styrene compound, and a vinylcompound.

Examples of the acrylic acid ester compound include methyl acrylate,ethyl acrylate, isopropyl acrylate, benzyl acrylate, naphthyl acrylate,anthryl acrylate, anthryl methyl acrylate, phenyl acrylate,2,2,2-trifluoroethyl acrylate, tert-butylacrylate, cyclohexyl acrylate,isobornyl acrylate, 2-methoxyethyl acrylate, methoxytriethylene glycolacrylate, 2-ethoxyethyl acrylate, tetrahydrofurfuryl acrylate,3-methoxybutyl acrylate, 2-methyl-2-adamantyl acrylate,2-propyl-2-adamantyl acrylate, 8-methyl-8-tricyclodecyl acrylate, and8-ethyl-8-tricyclodecyl acrylate.

Examples of the methacrylic acid ester compound include methylmethacrylate, ethyl methacrylate, isopropyl methacrylate, benzylmethacrylate, naphthyl methacrylate, anthryl methacrylate, anthrylmethylmethacrylate, phenyl methacrylate, 2,2,2-trifluoroethyl methacrylate,tert-butyl methacrylate, cyclohexyl methacrylate, isobornylmethacrylate, 2-methoxyethyl methacrylate, methoxy triethylene glycolmethacrylate, 2-ethoxy ethyl methacrylate, tetrahydrofurfurylmethacrylate, 3-methoxybutyl methacrylate, 2-methyl-2-adamanthylmethacrylate, 2-propyl-2-adamanthyl methacrylate,8-methyl-8-tricyclodecyl methacrylate, and 8-ethyl-8-tricyclodecylmethacrylate.

Examples of the maleimide compound include maleimide, N-methylmaleimide,N-phenyl maleimide, and N-cyclohexyl maleimide.

Examples of the styrene compound include styrene, methylstyrene,chlorostyrene, and bromostyrene.

Examples of the vinyl compound include vinyl ether, methylvinyl ether,benzylvinyl ether, phenylvinyl ether, and propylvinyl ether.

The amount of the monomer to be used, the monomer having the specificfunctional group 2 to be used to obtain the acrylic polymer that is anexample of the component (C), is preferably 2% by mole to 100% by molebased on the total amount of all monomers used to obtain the acrylicpolymer that is the component (C). When the monomer having the specificfunctional group 2 is excessively low, the alignment properties of acured film to be obtained is insufficient.

When the monomer that does not have the specific functional group 2 isused to obtain the acrylic polymer, the amount of the monomer to be usedis preferably equal to or lower than 98% by mole based on the totalamount of all monomers.

Although the method for obtaining the acrylic polymer that is an exampleof the component (C) is not limited to a particular method, the acrylicpolymer can be obtained, for example, by subjecting the monomer havingthe specific functional group 2, a monomer that does not have thespecific functional group 2 if desired, and a polymerization initiatoror the like to polymerization reaction in a solvent in which theycoexist at a temperature of 50° C. to 110° C. The solvent to be usedherein is not limited as long as the solvent can dissolve the monomerhaving the specific functional group 2, the monomer that does not havethe specific functional group 2 to be used if desired, and apolymerization initiator or the like. Specific examples thereof will begiven in the <Solvent> section described later.

The acrylic polymer being an example of the component (C) to be obtainedby the above-described method is generally in a state of being dissolvedin the solvent.

A solution of the acrylic polymer being an example of the component (C)obtained by the method is poured into diethyl ether, water, or the likewith stirring and the acrylic polymer is reprecipitated. The precipitatethus obtained is filtered and washed, and then is dried at roomtemperature or dried by beating under atmospheric pressure or reducedpressure. Thus, a powder of the acrylic polymer being an example of thecomponent (C) can be prepared. By this operation, the polymerizationinitiator and an unreacted monomer that coexist with the acrylic polymerbeing an example of the component (C) can be removed, and consequently,a powder of the purified acrylic polymer as an example of the component(C) can be obtained. If the acrylic polymer cannot be sufficientlypurified by one operation, the obtained powder may be redissolved in asolvent, followed by repeating the above-described operation.

The acrylic polymer being a preferred example of the component (C) has aweight-average molecular weight of preferably 3,000 to 200,000, morepreferably 4,000 to 150,000, and still more preferably 5,000 to 100,000.An excessively high weight-average molecular weight exceeding 200,000may reduce the solubility in solvent, so that the handling property maydeteriorate, and an excessively low weight-average molecular weightbelow 3,000 may cause insufficient curing during heat curing, so thatthe solvent resistance and the beat resistance may decrease.

Examples of the cyclodextrins being one preferred example of thehigh-molecular compound of the component (C) include cyclodextrins suchas α-cyclodextrin, β-cyclodextrin, and γ-cyclodextrin; methylatedcyclodextrins such as methyl-α-cyclodextrin, methyl-β-cyclodextrin, andmethyl-γ-cyclodextrin; and hydroxyalkyl cyclodextrins such ashydroxymethyl-α-cyclodextrin, hydroxymethyl-β-cyclodextrin,hydroxymethyl-γ-cyclodextrin, 2-hydroxyethyl-α-cyclodextrin,2-hydroxyethyl-γ-cyclodextrin, 2-hydroxyethyl-γ-cyclodextrin,2-hydroxypropyl-α-cyclodextrin, 2-hydroxypropyl-β-cyclodextrin,2-hydroxypropyl-γ-cyclodextrin, 3-hydroxypropyl-α-cyclodextrin,3-hydroxypropyl-β-cyclodextrin, 3-hydroxypropyl-γ-cyclodextrin,2,3-dihydroxypropyl-α-cyclodextrin, 2,3-dihydroxypropyl-β-cyclodextrin,and 2,3-dihydroxypropyl-γ-cyclodextrin. For example, the hydroxyalkylcyclodextrins are preferred.

Examples of the celluloses being one preferred example of thehigh-molecular compound of the component (C) include hydroxyalkylcelluloses such as hydroxyethyl cellulose and hydroxypropyl cellulose;hydroxyalkyl alkyl celluloses such as hydroxyethyl methyl cellulose,hydroxypropyl methyl cellulose, and hydroxyethyl ethyl cellulose; andcellulose. For example, the hydroxyalkyl celluloses such as hydroxyethylcellulose and hydroxypropyl cellulose are preferred.

Examples of the polyether polyol being one preferred example of thehigh-molecular compound of the component (C) include those obtained byadding propylene oxide, a polyethylene glycol, or a polypropyleneglycol, or the like, to polyhydric alcohols such as a polyethyleneglycol, a polypropylene glycol, propylene glycol, bisphenol A,triethylene glycol, and sorbitol. Specific examples of the polyetherpolyol include ADEKA polyether P-series, G-series, EDP-series,BPX-series, FC-series, and CM-series manufactured by ADEKA Corporation;and UNIOX (registered trademark) HC-40, HC-60, ST-30E, ST-40E, G-450,and G-750, UNIOL (registered trademark) TG-330, TG-1000, TG-3000,TG-4000, HS-1600D, DA-400, DA-700, and DB-400, and NONION (registeredtrademark) LT-221, ST-221, and OT-22 manufactured by NOF Corporation.

Examples of the polyester polyol being one preferred example of thehigh-molecular compound of the component (C) include those obtained bycausing polyhydric carboxylic acids such as adipic acid, sebacic acid,and isophthalic acid to react with dials such as ethylene glycol,propylene glycol, butylene glycol, a polyethylene glycol, and apolypropylene glycol. Specific examples of the polyester polyol includePOLYLITE (registered trademark) OD-X-286, OD-X-102, OD-X-355, OD-X-2330,OD-X-240, OD-X-668, OD-X-2108, OD-X-2376, OD-X-2044, OD-X-688,OD-X-2068, OD-X-2547, OD-X-2420, OD-X-2523, OD-X-2555, OD-X-2560manufactured by DIC corporation; and Polyol P-510, P-1010, P-2010,P-3010, P-4010, P-5010, P-6010, P-510, F-1010, F-2010, F-3010, P-1011,P-2011, P-2013, P-2030, N-2010, and PNNA-2016 manufactured by KurarayCo., Ltd.

Examples of the polycarbonate polyol being one preferred example of thehigh-molecular compound of the component (C) include those obtained bycausing a polyhydric alcohol such as trimethylolpropane and ethyleneglycol to react with diethyl carbonate, diphenyl carbonate, ethylenecarbonate, or the like. Specific examples of the polycarbonate polyolinclude PLACCEL (registered trademark) CD205, CD205PL, CD210, and CD220manufactured by Daicel Chemical Industries, Ltd.; and a polycarbonatediol C-590, C-1050, C-2050, C-2090, and C-3090 manufactured by KurarayCo., Ltd.

Examples of the polycaprolactone polyol being one preferred example ofhigh-molecular compound of the component (C) include those obtained bycausing ring-opening polymerization of ε-caprolactone, using apolyhydric alcohol such as trimethylolpropane and ethylene glycol as aninitiator. Specific examples of the polycaprolactone polyol includePOLYLITE (registered trademark) OD-X-2155, OD-X-640, and OD-X-2568manufactured by DIC Corporation; and PLACCEL (registered trademark) 205,L205AL, 205U, 208, 210, 212, L212AL, 220, 230, 240, 303, 305, 308, 312,and 320 manufactured by Daicel Chemical Industries, Ltd.

Examples of the phenol novolac resin being one preferred example of thehigh-molecular compound of the component (C) include phenol-formaldehydepolycondensates.

In the retardation material-forming resin composition of the presentinvention, the compound of the component (C) may be used in a form ofpowder or in a form of solution in which the purified powder isredissolved in a solvent described below.

In the retardation material-forming resin composition of the presentinvention, the component (C) may be used singly, or a plurality ofcompounds exemplified as the component (C) may be used as a mixture.

The content of the component (C) in the retardation material-formingresin composition of the present invention is preferably 0 part by massto 200 parts by mass, and more preferably 0 part by mass to 150 parts bymass, based on 100 parts by mass of the total amount of the resin of thecomponent (A), the cross-linking agent of the component (B), and thecompound of the component (E) and the monomer of the component (F)described later. When the content of the component (C) is excessivelyhigh, the photo-alignment properties may deteriorate.

<Component (D)>

The retardation material-forming resin composition of the presentembodiment can further contain a cross-linking catalyst as a component(D) in addition to the component (A), the component (B), and thecomponent (C).

The cross-linking catalyst that is the component (D) can be an acid orthermal acid generator, for example. This component (D) is effective inpromoting heat-curing reaction of formation of the cured film with theretardation material-forming resin composition of the present invention.

When an acid or acid generator is used as the component (D), thecomponent (D) is not limited as long as the component is a sulfonic acidgroup-containing compound, hydrochloric acid or a salt thereof, or acompound that thermally decomposes to generate an acid during prebakingor postbaking, that is, a compound that thermally decomposes to generatean acid at a temperature of 80° C. to 250° C.

Examples of such a compound include hydrochloric acid; and sulfonicacids such as methanesulfonic acid, ethanesulfonic acid, propanesulfonicacid, butanesulfonic acid, pentanesulfonic acid, octanesulfonic acid,benzenesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid,trifluoromethanesulfonic acid, p-phenolsulfonic acid,2-naphthalenesulfonic acid, mesitylenesulfonic acid, p-xylene-2-sulfonicacid, m-xylene-2-sulfonic acid, 4-ethylbenzenesulfonic acid,1H,1H,2H,2H-perfluoroctanesulfonic acid,perfluoro(2-ethoxyethane)sulfonic acid, pentafluoroethanesulfonic acid,nonafluorobutane-1-sulfonic acid, and dodecylbenzenesulfonic acid, and ahydrate or a salt thereof.

Examples of the compound generating an acid by heat includebis(tosyloxy)ethane, bis(tosyloxy)propane, bis(tosyloxy)butane,p-nitrobenzyl tosylate, o-nitrobenzyl tosylate, 1,2,3-phenylenetris(methylsulfonate), p-toluenesulfonic acid pyridinium salt,p-toluenesulfonic acid morphonium salt, p-toluenesulfonic acid ethylester, p-toluenesulfonic acid propyl ester, p-toluenesulfonic acid butylester, p-toluenesulfonic acid isobutyl ester, p-toluenesulfonic acidmethyl ester, p-toluenesulfonic acid phenethyl ester, cyanomethylp-toluenesulfonate 2,2,2-trifluoroethyl p-toluenesulfonate,2-hydroxybutyl p-toluenesulfonate, and N-ethyl-p-toluenesulfonamide.

Examples of commercially available products of the compound thatgenerates an acid by heat include TA100, TA120, and TA160 (manufacturedby San-Apro Ltd.); K-PURE [registered trademark] TAG2689, K-PURETAG2690, K-PURE CXC1614, and K-PURE CXC1738 (manufactured by Kingindustries Inc.); and San-Aid SI-100L and San-Aid SI-180L (manufacturedby Sanshin Chemical Industry Co., Ltd.).

Other examples of the cross-linking catalyst that is the component (D)include a metal chelate compound and a silanol compound. Use of themetal chelate compound and the silanol compound in combination as thecomponent (D) is effective in promoting heat-curing reaction of a curedfilm formed of the retardation material-forming resin composition of thepresent invention.

Examples of the metal chelate compound include a zirconium compound, atitanium compound, and an aluminum compound, and more specificallyinclude diisopropyl titanium diacetylacetonate, titaniumtetraacetylacetonate, zirconium tetraacetylacetonate, diisopropoxyethylacetoacetate aluminum, diisopropoxy acetylacetonate aluminum,isopropoxy bis(ethylacetoacetate) aluminum, isopropoxybis(acetylacetonate) aluminum tris(ethylacetoacetate) aluminum,tris(acetylacetonate) aluminum [tris(2,4-pentanedionato) aluminum(III)],and monoacetylacetonate bis(ethylacetoacetate) aluminum.

Examples of the silanol compound include triphenyl silanol, trimethylsilanol, triethyl silanol, 1,1,3,3-tetraphenyl-1, 3-disiloxanediol, and1,4-bis(hydroxydimethylsilyl)benzene.

The content of the component (D) in the retardation material-formingresin composition of the present invention is preferably 0 part by massto 20 parts by mass, more preferably 0 part by mass to 15 parts by mass,and further preferably 0 part by mass to 10 parts by mass, with respectto 100 parts by mass of the total amount of the resin of the component(A), the cross-linking agent of the component (B), the compound of thecomponent (C), and the compound of the component (F) and the monomer ofthe component (F) described later. When the content of the component (D)is higher than 20 parts by mass, the preservation stability of thecomposition may deteriorate.

<Component (E)>

The retardation material-forming resin composition of the presentinvention may contain, as the component (E), a compound having a groupthat can thermally cross-link with any of the component (A), thecomponent (B) and the component (C), and a polymerizable group, that is,a compound having one or more polymerizable groups and at least onegroup A selected from the group consisting of hydroxy group, carboxygroup, amide group, amino group, an alkoxysilyl group, and a group ofFormula (2) or one or more groups that react with the at least one groupA.

When a cured film formed of the retardation material-forming resincomposition of the present invention containing the component (E) isused as an orientation material, the compound of the component (E)enhances adhesion between the cured film and a layer of polymerizableliquid crystal formed and cured on the cured film, and thus functions asan adhesion-enhancing component.

Preferred examples of the compound of the component (E) include acompound having a polymerizable group containing a C═C double bond andhydroxy group and a compound having a polymerizable group containing aC═C double bond and ran N-alkoxymethyl group. Examples of thepolymerizable group containing a C═C double bond include acrylic group,methacrylic group, vinyl group, an allyl group, and maleimide group.

Preferred examples of the compound of the component (E) having apolymerizable group containing a C═C double bond and hydroxy groupinclude compounds below. However, the compound of the component (E) isnot limited to these exemplified compounds.

(In the Formulae, R⁴¹ is a hydrogen atom or methyl group; and m is aninteger of 1 to 10.)

In the compound having a polymerizable group containing a C═C doublebond and an N-alkoxymethyl group as the component (E), examples of anitrogen atom N of the N-alkoxymethyl group include a nitrogen atom ofamide, a nitrogen atom of thioamide, a nitrogen atom of urea, a nitrogenatom of thiourea, a nitrogen atom of urethane, and a nitrogen atombonded to a vicinal position of a nitrogen atom of a nitrogen-containinghetero ring. Thus, examples of the N-alkoxymethyl group include astructure in which an alkoxymethyl group binds to a nitrogen atomselected from a nitrogen atom of amide, a nitrogen atom of thioamide, anitrogen atom of urea, a nitrogen atom of thiourea, a nitrogen atom ofurethane, a nitrogen atom bonded to a vicinal position of a nitrogenatom of a nitrogen-containing hetero ring, and the like.

The compound having a polymerizable group containing a C═C double bondand an N-alkoxymethyl group as the component (E) only needs to have thegroup described above, and preferred examples thereof include a compoundof Formula (X):

(In the Formula, R¹ is a hydrogen atom or methyl group; and R² is ahydrogen atom or a linear or branched alkyl group having a carbon atomnumber of 1 to 10.)

Examples of the alkyl group include methyl group, ethyl group, n-propylgroup, isopropyl group, n-butyl group, isobutyl group, sec-butyl group,tert-butyl group, n-pentyl group, 1-methyl-n-butyl group,2-methyl-n-butyl group, 3-methyl-n-butyl group, 1,1-dimethyl-n-propylgroup, 1,2-dimethyl-n-propyl group, 2,2-dimethyl-n-propyl group,1-ethyl-n-propyl group, n-hexyl group, 1-methyl-n-pentyl group,2-methyl-n-pentyl group, 3-methyl-n-pentyl group, 4-methyl-n-pentylgroup, 1,1-dimethyl-n-butyl group, 1,2-dimethyl-n-butyl group,1,3-dimethyl-n-butyl group, 2,2-dimethyl-n-butyl group,2,3-dimethyl-n-butyl group, 3,3-dimethyl-n-butyl group, 1-ethyl-n-butylgroup, 2-ethyl-n-butyl group, 1,1,2-trimethyl-n-propyl group,1,2,2-trimethyl-n-propyl group, 1-ethyl-1-methyl-n-propyl group,1-ethyl-2-methyl-n-propyl group, n-heptyl group, 1-methyl-n-hexyl group,2-methyl-n-hexyl group, 3-methyl-n-hexyl group, 1,1-dimethyl-n-pentylgroup, 1,2-dimethyl-n-pentyl group, 3-dimethyl-n-pentyl group,2,2-dimethyl-n-pentyl group, 2,3-dimethyl-n-pentyl group,3,3-dimethyl-n-pentyl group, 1-ethyl-n-pentyl group, 2-ethyl-n-pentylgroup, 3-ethyl-n-pentyl group, 1-methyl-1-ethyl-n-butyl group,1-methyl-2-ethyl-n-butyl group. 1-ethyl-2-methyl-n-butyl group,2-methyl-2-ethyl-n-butyl group, 2-ethyl-3-methyl-n-butyl group, n-octylgroup, 1-methyl-n-heptyl group, 2-methyl-n-heptyl group,3-methyl-n-heptyl group, 1,1-dimethyl-n-hexyl group,1,2-dimethyl-n-hexyl group, 1,3-dimethyl-n-hexyl group,2,2-dimethyl-n-hexyl group, 2,3-dimethyl-n-hexyl group,3,3-dimethyl-n-hexyl group, 1-ethyl-n-hexyl group, 2-ethyl-n-hexylgroup, 3-ethyl-n-hexyl group, 1-methyl-1-ethyl-n-pentyl group,1-methyl-2-ethyl-n-pentyl group, 1-methyl-3-ethyl-n-pentyl group,2-methyl-2-ethyl-n-pentyl group, 2-methyl-3-ethyl-n-pentyl group,3-methyl-3-ethyl-n-pentyl group, n-nonyl group, and n-decyl group.

Specific examples of the compound of Formula (X) include N-butoxymethylacrylamide, N-isobutoxymethyl acrylamide, N-methoxymethyl acrylamide,N-methoxymethyl methacrylamide, and N-methylol acrylamide.

Preferred examples of the compound having a polymerizable groupcontaining a C═C double bond and an N-alkoxymethyl group as thecomponent (E) in another aspect include a compound of Formula (X2):

(in the Formula, R¹¹ is a hydrogen atom or methyl group. R¹³ and R¹⁴ areindependently a linear or branched alkylene group having a carbon atomnumber of 2 to 20, a C₅₋₆ aliphatic-ring group, or a C₅₋₆ aliphaticring-containing aliphatic group, and in these groups, one methylenegroup or a plurality of unadjacent methylene groups may each be replacedwith an ether bond. R¹² is a linear or branched alkyl group having acarbon atom number of 1 to 20, a C₅₋₆ aliphatic-ring group, or a C₅₋₆aliphatic ring-containing aliphatic group, and in these groups, onemethylene group or a plurality of unadjacent methylene groups may eachbe replaced with an ether bond. Z is >NCOO— or —OCON< (herein, “—”indicates that the number of bonding hands is one. “>” and “<” indicatethat the number of bonding hands is two and either one bonding handbinds to —CH₂OR¹²). “r” is a natural number of two to nine.)

Specific examples of the C₂₋₂₀ alkylene group in the definition of R¹³and R¹⁴ include a group with a valence of two to nine obtained byfurther removing one to eight hydrogen atoms from a C₂₋₂₀ alkyl group.

Specific examples of the C₂₋₂₀ alkyl group include ethyl group, n-propylgroup, i-propyl group, n-butyl group, i-butyl group, s-butyl group,t-butyl group, n-pentyl group, 1-methyl-n-butyl group, 2-methyl-n-butylgroup, 3-methyl-n-butyl group, 1,1-dimethyl-n-propyl group, n-hexylgroup, 1-methyl-n-pentyl group, 2-methyl-n-pentyl group, 1,1-dimethyl-n-butyl group, 1-ethyl-n-butyl group, 1,1,2-trimethyl-n-propylgroup, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group,n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group,n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecylgroup, n-nonadecyl group, n-eicosyl group, cyclopentyl group, cyclohexylgroup, groups in which one or more out of these groups are bonded withina range of up to C₂₀, and groups in which one methylene group or aplurality of unadjacent methylene groups are each replaced with an etherbond.

Among the groups given above, R¹³ and R¹⁴ are each preferably a C₂₋₁₀alkylene group and it is particularly preferable that R¹³ be ethylenegroup and R¹⁴ be hexylene group from the viewpoint of availability ofraw material, for example.

Specific examples of the C₁₋₂₀ alkyl group in the definition of R¹²include the specific examples of the C₂₋₂₀ alkyl group and methyl group.Among them, the C₁₋₆ alkyl group is preferred, and the methyl group, theethyl group, the n-propyl group, and the n-butyl group are particularlypreferred.

Examples of r include natural numbers of two to nine, and among them,two to six are preferred.

The compound (X2) is obtained by a production method illustrated in areaction scheme below. Specifically, the compound (X2) is produced bysubjecting a carbamate compound (hereinafter, also called “compound(X2-1)”) of Formula (X2-1) having acrylic group or methacryl group toreaction in a solvent into which trimethylsilyl chloride andparaformaldehyde are added to synthesize an intermediate of Formula(X2-2), and adding alcohol of R¹²—OH to this reaction solution, therebycausing the solution to react.

In the Formulae, R¹¹, R¹², R¹³, R¹⁴, Z, and r are those described above;and X is —NHCOO— or —OCONH—.

Although the amount of trimethylsilyl chloride and paraformaldehyde tobe used to the compound (X2-1) is not limited to a particular amount, inorder to complete the reaction, with respect to one carbamate bond in amolecule, 1.0 equivalent to 6.0 equivalents of trimethylsilyl chlorideis preferably used, and 1.0 equivalent to 3.0 equivalents ofparaformaldehyde is preferably used, in which the equivalents oftrimethylsilyl chloride to be used are preferably larger than theequivalents of paraformaldehyde to be used.

The reaction solvent is not limited as long as the solvent is inert toreaction, and examples thereof include hydrocarbons such as hexane,cyclohexane, benzene, and toluene; halogenated hydrocarbons such asmethylene chloride, carbon tetrachloride, chloroform, and1,2-dichloroethane; ethers such as diethyl ether, diisopropyl ether,1,4-dioxane, and tetrahydrofuran; nitriles such as acetonitrile andpropionitrile; a nitrogen-containing aprotic polar solvent such asN,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone,and 1,3-dimethyl-2-imidazolidinone; and pyridines such as pyridine andpicoline. These solvents may be used singly or in combination of two ormore of them. Methylene chloride and chloroform are preferred, andmethylene chloride is more preferred.

Although the amount (the reaction concentration) of the solvent to beused is not limited to a particular value, the reaction may be performedwithout the solvent, or the solvent may be used in an amount of 0.1 to100 times by mass the amount of the compound (X2-1). The amount to beused is preferably 1 to 30 times by mass, and more preferably 2 to 20times by mass.

Although the reaction temperature is not limited to a particulartemperature, the reaction temperature is −90° C. to 200° C., preferably−20° C. to 100° C., and more preferably −10° C. to 50° C.

The reaction time is generally 0.05 hours to 200 hours, and preferably0.5 hours to 100 hours.

The reaction can be performed under atmospheric pressure or increasedpressure, and may be performed in a batch process or in a continuousprocess.

When the reaction is performed, a polymerization inhibitor may be added.As the polymerization inhibitor, BHT (2,6-di-tert-butyl-para-cresol),hydroquinone, para-methoxyphenol, or the like can be used, and any agentthat inhibits polymerization of acrylic group or methacrylic group maybe used without being limited.

Although the addition amount of the polymerization inhibitor to be addedis not limited to a particular value, the addition amount is preferably0.0001wt % to 10 wt %, and preferably 0.01 wt % to 1 wt % with respectto total amount (mass) of the compound (X2-1) to be used. In the presentspecification, wt % means % by mass.

In the process of causing the intermediate (X2-2) to react with alcohol,a base may be added in order to surpress hydrolysis under acidicconditions. Examples of the base include pyridines such as pyridine andpicoline; and tertiary amines such as trimethylamine, triethylamine,diisopropylethylamine, and tributylamine. Triethylamine anddiisopropylethylamine are preferred, and triethylamine is morepreferred. Although the addition amount of the base to be added is notlimited to a particular value, the addition amount is preferably 0.01equivalents to 2.0 equivalents, and more preferably 0.5 equivalents to1.0 equivalent with respect to the addition amount of the trimethylsilylchloride used during the reaction.

After the intermediate (X2-2) is obtained from the compound (X2-1),without isolating the intermediate (X2-2), alcohol may be added theretofor reaction.

Although the method for synthesizing the compound (X2-1) is not limitedto a particular method, the compound (X2-1) can be produced by causing a(meth)acryloyloxyalkyl isocyanate to react with a polyol compound, orcausing a hydroxyalkyl (meth)acrylate compound to react with apolyisocyanate compound.

Specific examples of the (meth)acryloyloxyalkyl isocyanate include2-methacryloyloxyethyl isocyanate (trade name: Karenz MOI [registeredtrademark] manufactured by Showa Denko K.K.) and 2-acryloyloxyethylisocyanate (trade name: Karenz AOI [registered trademark] manufacturedby Showa Denko K.K.).

Specific examples of the polyol compound include a diol compound such asethylene glycol, propylene glycol, 1,4-butanediol, 1,3-butanediol,1,5-pentanediol, neopentylglycol, 3-methyl-1,5-pentanediol,1,6-hexanediol and 1,4-cyclohexane dimethanol; a triol compound such asglycerin and trimethylolpropane; pentaerythritol; dipentaerythritol; anddiglycerine.

Specific examples of the hydroxyalkyl (meth)acrylate compound include amonomer having hydroxy group such as 2-hydroxyethyl acrylate,2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropylmethacrylate, 4-hydroxybutyl acrylate, 4-hydroxybutyl methacrylate,diethylene glycol monoacrylate, diethylene glycol monomethacrylate, apoly(ethylene glycol)ethylether acrylate, and a poly(ethyleneglycol)ethylether methacrylate.

Specific examples of the polyisocyanate compound include aliphaticdiisocyanates such as hexamethylene diisocyanate, 2,4,4-trimethylhexamethylene diisocyanate, and dimer acid diisocyanate; alicyclicdiisocyanates such as isophorone diisocyanate, 4,4′-methylenebis(cyclohexyl isocyanate) and ω,ω′-diisocyanate dimethylcyclohexane;triisocyanates such as lysine ester triisocyanate, 1,6,11-undecanetriisocyanate, 1,8-diisocyanate-4-isocyanate methyloctane,1,3,6-hexamethylene triisocyanate, and bicycloheptane triisocyanate.

The (meth)acryloyloxyalkyl isocyanate compound, the polyol compound, thehydroxyalkyl (meth)acrylate compound, and the polyisocyanate compoundare generally commercially available, and can also be synthesized by aknown method.

In the retardation material-forming resin composition of the presentinvention, the component (E) may be a mixture of a plurality ofcompounds of the component (E).

When the cured film formed of the retardation material-forming resincomposition of the present invention containing the component (E) isused as a liquid crystal alignment film, the compound of the component(E), such that adhesion between the liquid crystal alignment film (curedfilm) and a layer of polymerizable liquid crystal formed thereon isenhanced, can link a polymerizable functional group of the polymerizableliquid crystal with a cross-linking reaction moiety contained in theliquid crystal alignment film by covalent bonding. Consequently, theretardation material of the present embodiment that is formed bylaminating the polymerizable liquid crystal cured on the orientationmaterial of the present embodiment can retain excellent adhesion evenunder high-temperature and high-humidity conditions, and can have highdurability against peeling or the like.

The content of the component (E) in the retardation material-formingresin composition of the present invention is preferably 0 part by massto 80 parts by mass, and more preferably 0 part by mass to 50 parts bymass with respect to 100 parts by mass of the total amount of the resinof the component (A), the cross-linking agent of the component (B), thecompound of the component (C), the cross-linking catalyst of thecomponent (D), and the monomer of the component (F) described later.When the content of the component (E) is higher than 80 parts by mass,the photo-alignment properties and the solvent resistance of the curedfilm may deteriorate.

<Component (F)>

The retardation material-forming resin composition of the presentinvention may contain, as the component (F), a monomer having aphoto-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group and one or more polymerizablegroups.

When a cured film formed of the retardation material-forming resincomposition of the present invention containing the monomer of thecomponent (F) is used as an orientation material, this monomer enhancesadhesion between the cured film and a layer of polymerizable liquidcrystal formed and cured on the cured film, and thus functions as anadhesion-enhancing component.

The photo-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group in the monomer of thecomponent (F) has been described (supra).

The monomer of the component (F) is preferably a monomer having thephoto-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group and a polymerizable groupcontaining a C═C double bond.

The photo-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group is preferably an organic groupincluding a structure of Formula (1):

(in the Formula, R is a hydroxy group, an amino group, a hydroxyphenoxygroup, a carboxyphenoxy group, an aminophenoxy group, an aminocarbonylphenoxy group, a phenylamino group, a hydroxy phenylamino group, acarboxy phenylamino group, an amino phenylamino group, a hydroxy alkylamino group, or a bis(hydroxyalkyl)amino group; and X¹ is a phenylenegroup that is optionally substituted with an optional substituent, inwhich a benzene ring in the definition of these substituents isoptionally substituted with a substituent).

The optional substituent has been described in (supra), and thesubstituent with which the benzene ring is optionally substituted hasbeen described described (supra).

Among them, an organic group that includes a structure of Formula (1) inwhich R is a hydroxy group or an amino group, and X¹ is a phenylenegroup that is optionally substituted with an optional substituent ispreferred.

Examples of the polymerizable group containing a C═C double bond includeacrylic group, methacrylic group, vinyl group, an allyl group, andmaleimide group.

Examples of the monomer of the component (F) include4-(6-methacryloxyhexyl-1-oxy)cinnamic acid,4-(3-methacryloxypropyl-1-oxy)cinnamic acid, and4-(6-methacryloxyhexyl-1-oxy)cinnamamide.

The content of the component (F) in the retardation material-formingresin composition of the present invention is preferably 0 part by massto 40 parts by mass, and more preferably 0 part by mass to 30 parts bymass with respect to 100 parts by mass of the resin of the component(A), the cross-linking agent of the component (B), the compound of thecomponent (C), and the cross-linking catalyst of the component (D). Whenthe content of the component (F) is higher than 40 parts by mass, thesolvent resistance of the cured film may deteriorate.

<Solvent>

The retardation material-forming resin composition of the presentinvention is mainly used in a solution state of being dissolved in asolvent. The type, the structure, and the like of the solvent usedherein are not limited as long as the solvent can dissolve the component(A) and the component (B), and if desired, the component (C), thecomponent (D), the component (E), the component (F), and/or otheradditives described later.

Specific examples of the solvent include methanol, ethanol, n-propanol,isopropanol (2-propanol), n-butanol, isobutanol, n-pentanol,2-methyl-1-butanol, ethylene glycol monomethyl ether, ethylene glycolmonoethyl ether, methylcellosolve acetate, ethylcellosolve acetate,diethylene glycol monomethyl ether, diethylene glycol monoethyl ether,propylene glycol, diethylene glycol, propylene glycol monomethyl ether,propylene glycol monomethyl ether acetate, propylene glycol monoethylether, propylene glycol propyl ether, propylene glycol propyl etheracetate, toluene, xylene, methyl ethyl ketone, cyclopentanone,cyclohexanone, 2-butanone, methyl isobutyl ketone, 3-methyl-2-pentanone,2-pentanone, 2-heptanone, γ-butyrolactone, ethyl 2-hydroxypropionate,ethyl 2-hydroxy-2-methylpropionate, ethyl ethoxyacetate ethylhydroxyacetate, methyl 2-hydroxy-3-methylbutanoate, methyl3-methoxypropinoate, ethyl 3-methoxypropionate, ethyl3-ethoxypropionate, methyl 3-ethoxypropionate, methyl pyruvate, ethylpyruvate, ethyl acetate, butyl acetate, ethyl lactate, butyl lactate,cyclopentyl methyl ether, N,N-dimethylformamide, N,N-dimethylacetamide,and N-methylpyrrolidone.

When a cured film is formed with the retardation material-forming resincomposition of the present invention on a film to produce an orientationmaterial, methanol, ethanol, isopropanol, n-propanol, n-butanol,2-methyl-1-butanol, 2-heptanone, methyl isobutyl ketone, propyleneglycol monomethyl edict propylene diethylene glycol, and propyleneglycol monomethyl ether acetate are preferred because the film exhibitsresistance against these solvents.

These solvents may be used singly or in combination of two or more ofthem.

<Other Additives>

Furthermore, the retardation material-forming resin composition of thepresent invention may contain, as long as not impairing the effects ofthe present invention and if necessary, a sensitizer, anadhesion-enhancing agent, a silane coupling agent, a surfactant, atheology adjusting agent, a pigment, a dye, a preservation stabilizer,an antifoamer, an antioxidant, and the like.

For example, the sensitizer is effective in promoting photoreactionafter a thermally cured film is formed a with the retardationmaterial-forming resin composition of the present invention.

Examples of the sensitizer being one example of other additives includebenzophenone, anthracene, anthraquinone, thioxanthone, derivativesthereof, and a nitrophenyl compound. Among them, a benzophenonederivative and a nitrophenyl compound are preferred. Specific examplesof the preferred compound include N,N-diethylamino benzophenone,2-nitrofluorene, 2-nitrofluorenone, 5-nitroacenaphthene,4-nitrobiphenyl, 4-nitrocinnamic acid, 4-nitrostilbene,4-nitrobenzophenone, and 5-nitroindole. In particular, N,N-diethylaminobenzophenone that is a derivative of benzophenone is preferred.

These sensitizers are not limited to those given above. The sensitizermay be used singly or in combination of two or more compounds.

The proportion of sensitizer to be used in the retardationmaterial-forming resin composition of the present invention ispreferably 0.1 parts by mass to 20 parts by mass, and more preferably0.2 parts by mass to 10 parts by mass with respect to 100 parts by massof the total mass of the component (A) to the component (F). When thisproportion is excessively low, the effect as a sensitizer is notsufficiently obtained in some cases, and when the proportion isexcessively high, decrease of the transmittance and roughening of thecoating film may occur.

<Preparation of Retardation Material-Forming Resin Composition>

The retardation material-forming resin composition of the presentinvention contains a resin that is the component (A) and a cross-linkingagent that is the component (B). In addition to the component (A) andthe component (B), the retardation material-forming resin composition ofthe present invention may further contain: as the component (C), acompound having at least two groups A selected from the group consistingof hydroxy group, carboxy group, amide group, amino group, analkoxysilyl group, and a group of Formula (2); a cross-linking catalystas the component (D); as the component (E), a compound having one ormore polymerizable groups and at least one group A selected from thegroup consisting of hydroxy group, carboxy group, amide group, aminogroup, an alkoxysilyl group, and a group of formula (2), or one or moregroups that react with the at least one group A and as the component(F), a monomer having a photo-aligning group to which a thermallyreactive moiety is bonded directly or connected via a linking group andone or more polymerizable groups. As long as the effects of the presentinvention are not impaired, the retardation material-forming resincomposition of the present invention may contain other additives.

The blending ratio of the component (A) to the component (B) ispreferably 20:80 to 100:0 in mass ratio. When the content of thecomponent (B) is excessively high, the liquid crystal alignmentproperties are prone to deteriorate.

Preferred examples of the retardation material-forming resin compositionof the present invention are listed below.

[1]: A retardation material-forming resin composition that contains thecomponent (A).

[2]: A retardation material-forming resin composition that contains thecomponent (C) at a content of 0 part by mass to 100 parts by mass basedon 100 parts by mass of the component (A).

[3]: A retardation material-forming resin composition in which theblending ratio of the component (A) to the component (B) is 20:80 to100:0 in mass ratio and that contains the component (C) at a content of0 to 100 parts by mass based on 100 parts by mass of the total amount ofthe component (A) and the component (B).

[4]: A retardation material-forming resin composition that contains thecomponent (C) at a content of 0 part by mass to 100 parts by mass basedon 100 parts by mass of the total amount of the component (A) and thecomponent (B), and a solvent.

[5]: A retardation material-forming resin composition that contains thecomponent (C) at a content of 0 part by mass to 100 parts by mass andthe component (D) at a content of 0 part by mass to 10 parts by massbased on 100 parts by mass of the total amount of the component (A) andthe component (B), and a solvent.

[6]: A retardation material-forming resin composition that contains thecomponent (C) at a content of 0 part by mass to 100 parts by mass, thecomponent (D) at a content of 0 part by mass to 10 parts by mass, andthe component (E) at a content of 0 part by mass to 50 parts by massbased on 100 parts by mass of the total amount of the component (A) andthe component (B), and a solvent.

[7]: A retardation material-forming resin composition that contains thecomponent (C) at a content of 0 part by mass to 100 parts by mass, thecomponent (D) at a content of 0 part by mass to 10 parts by mass, thecomponent (E) at a content of 0 part by mass to 50 parts by mass, andthe component (F) at a content of 0 part by mass to 40 parts by massbased on 100 parts by mass of the total amount of the component (A) andthe component (B), and a solvent.

The blending proportion, a preparation method, and the like, when theretardation material-forming resin composition of the present inventionis used as a solution will be described below in detail.

The proportion of solid content in the retardation material-formingresin composition of the present invention is, but not limited to aparticular proportion as long as each component is uniformly dissolvedin a solvent, 1% by mass to 80% by mass, preferably 2% by mass to 60% bymass, and more preferably 3% by mass to 40% by mass. The solid contentherein is a component remaining after excluding the solvent from thewhole component of the retardation material-forming resin composition.

The preparation method of the retardation material-forming resincomposition of the present invention is not limited to a particularmethod. Examples of the preparation method include a method in which thecomponent (B), the component (C), the component (D), and further thecomponent (E), and the component (F) and the like are mixed in asolution of the component (A) dissolved in a solvent at predeterminedproportions, and in a method of making this solution uniform or in acertain step of this preparation method, other additives are furtheradded therein if necessary, and the resulting solution is mixed.

In the preparation of the retardation material-forming resin compositionof the present invention, a solution of the specific copolymer obtainedby copolymerization reaction in the solvent can be used without beingprocessed. In this case, for example, into a solution of the component(A), the component (B), the component (C), the component (D), thecomponent (E), the component (F), and the like, are mixed in the samemanner described above, and the resulting solution is made uniform. Atthis time, a solvent may be further added thereto for the purpose ofadjusting the concentration. In this case, the solvent to be used in theprocess of preparing the component (A) may be the same as or may bedifferent from the solvent to be used for adjusting the concentration ofthe retardation material-forming resin composition.

It is preferable that the solution of the retardation material-formingresin composition thus prepared be used after being filtered with afilter having a pore diameter of about 0.2 μm.

<Cured Film, Orientation Material, and Retardation Material>

A cured film can be formed as follows: the solution of the retardationmaterial-forming resin composition of the present invention is appliedonto a substrate (for example, a silicon/silicon dioxide coatedsubstrate, a silicon nitride substrate, a substrate coated with a metalsuch as aluminum, molybdenum, and chromium, a glass substrate, a quartzsubstrate, and an ITO substrate) or a film (for example, a resin filmsuch as a triacetylcellulose (TAC) film, a cycloolefin polymer film, apoly ethylene terephthalate film, and an acrylic film), and the like, bybar coating, rotation coating, flow coating, roll coating, slit coating,slit coating followed by rotation coating, inkjet coating, printing, orthe like, to form a coating; and then the resultant coating is heatedand dried on a hot plate or in an oven.

As a condition for the beating and drying, it is preferable thatcross-linking reaction with a cross-linking agent proceed in such amanner that a component of an orientation material to be formed of thecured film is not eluted into a polymerizable liquid crystal solution tobe applied onto the orientation material. For example, a heatingtemperature and a heating time that are appropriately selected from atemperature range of 60° C. to 230° C. and a time range of 0.4 minutesto 60 minutes are used. The heating temperature and the heating time arepreferably 70° C. to 230° C. and 0.5 minutes to 10 minutes.

The film thickness of the cured film to be formed of the retardationmaterial-forming resin composition of the present invention is 0.05 μmto 5 μm, for example, which can be appropriately selected inconsideration of level differences and the optical and electricalproperties of a substrate to be used.

When irradiated with polarized UV light, the cured film thus formed canfunction as an orientation material, that is, a member in which acompound having liquid crystallinity including liquid crystals isaligned.

As a method for irradiation with polarized UV light, ultraviolet lightto visible light having a wavelength of 150 nm to 450 nm are generallyused, and the irradiation is performed by radiating linear polarizedlight in a vertical direction or an oblique direction at roomtemperature or in a heated state.

The orientation material formed of the retardation material-formingresin composition of the present invention has solvent resistance andheat resistance. Thus, after a retardation substance including apolymerizable liquid crystal solution is applied onto the orientationmaterial, the retardation substance is heated up to the phase transitiontemperature of the liquid crystal, whereby the retardation substance istransformed into a liquid crystal state to be aligned on the orientationmaterial. The retardation substance thus aligned is cured without beingprocessed, whereby the retardation material as a layer having opticalanisotropy can be formed.

As the retardation substance, for example, a liquid crystal monomerhaving a polymerizable group and a composition containing the liquidcrystal monomer are used. When the substrate forming the orientationmaterial is a film, the film having the retardation material of thepresent embodiment is useful as a retardation film. Some of suchretardation substances for forming retardation materials are transformedinto a liquid crystal state to be aligned in a state of horizontalalignment, cholesteric alignment, vertical alignment, hybrid alignment,or the like, on the orientation material, and thus can be useddifferently depending on the respective retardation required.

When a patterned retardation material to be used for a 3D display isproduced, a cured film that is formed of the retardationmaterial-forming resin composition of the present embodiment by theabove-described method is irradiated with polarized UV light in adirection of +45 degrees, for example, from a predetermined referencethrough a line-and-space pattern mask, and the cured film is thenirradiated with polarized light in a direction of −45 degrees afterremoving the mask. Thus, an orientation material is obtained in whichtwo types of liquid crystal alignment regions are formed and thedirections of alignment control of liquid crystals in the regions aredifferent from each other. Subsequently, a retardation substanceincluding a polymerizable liquid crystal solution is applied onto theorientation material, and is then heated up to the phase transitiontemperature of the liquid crystal. Thus, the retardation substance istransformed into a liquid crystal state and aligned on the orientationmaterial. The retardation substance in which this alignment state isachieved is cured without being processed. Thus, the patternedretardation material can be obtained in which two types of retardationregions having different retardation properties are regularly alignedeach in plurality.

Two substrates having orientation materials of the present invention,which have been formed as described above, are used, and the substratesare stuck together with spacer interposed therebetween such that theorientation materials on the respective substrates face each other.Subsequently, a liquid crystal is injected between the substrates,whereby a liquid crystal display element in which they liquid crystal isaligned can be produced.

Thus, the retardation, material-forming resin composition of the presentinvention can be suitably used for producing various retardationmaterials (retardation films) or liquid crystal display elements.

[Cured-Film Formation Composition]

The present invention also relates to a cured-film formation compositionthat contains a resin having the specific photo-aligning group as thecomponent (A). In addition to the component (A), the cured-filmformation composition of the present invention may contain across-linking agent as the component (B). Furthermore, in addition tothe component (A) and the component (B), the cured-film formationcomposition of the present invention may further contain, as thecomponent (C), a compound having at least two groups A selected from thegroup consisting of hydroxy group, carboxy group, amide group, aminogroup, an alkoxysilyl group, and a group of Formula (2):

(in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup).

The cured-film formation composition of the present invention maycontain other additives as long as the effects of the present inventionare not impaired.

A preparation method and the like of the component (A) to the component(C) and the cured-film formation composition are the same as those ofthe retardation material-forming resin composition described above.

EXAMPLES

The present embodiment will be described in further detail withreference to Examples below. The present invention is, however, notlimited to these Examples.

[Composition Components and Abbreviations thereof to be used inExamples, etc.]

The respective composition components to be used in Examples andComparative Examples below are as follows.

<Component (A), Component (B), Component (C): Polymer Raw Material>

-   M6CA: 4-(6-methacryloxyhexyl-1-oxy)cinnamic acid-   M3CA: 4-(3-methacryloxypropyl-1-oxy)cinnamic acid-   M6CAm: 4-(6-methacryloxyhexyl-1-oxy)cinnamamide-   HEMA: 2-hydroxyethyl methacrylate-   MAA: methacrylic acid-   MMA: methyl methacrylate-   Karenz MOI-BM (registered trademark):-   2-(0-(1′-methylpropylideneamino)carboxyamino)ethyl methacrylate    (manufactured by Showa Denko K.K.)-   BMAA: N-butoxymethyl acrylamide-   St: styrene-   EGAMA: ethylene glycol mono-acetoacetate monomethacrylate    (2-acetoacetoxy ethyl methacrylate)

-   M100: CYCLOMER (registered trademark) M100 manufactured by Daicel    Corporation

-   AIBN: α,α′-azobisisobutyronitrile

<Component (B): Cross-Linking Agent>

-   HMM: melamine cross-linking agent [CYMEL (registered trademark) 303    (manufactured by Mitsui Cytec Ltd.] of the structural formula:

-   TC-401: titanium tetraacetylacetonate (containing IPA [isopropanol]    as a solvent at 35%) OLGATIX (registered trademark) TC-401    manufactured by Matsumoto Fine Chemical Co., Ltd.

<Component (D): Cross-Linking Catalyst Component>

-   PTSA: p-toluenesulfonic acid

-   TPDA: tris(2,4-pentanedionato)-aluminum(III)-   TPS: triphenyl silanol-   TAG-2689: K-PURE (registered trademark) TAG2689 (manufactured by    King Industries Inc.)

<Component (E): Adhesive Component>

-   80MFA: epoxyester 80MFA (manufactured by Kyoeisha Chemical Co., Ltd)-   BMAA: N-butoxymethyl acrylamide

<Component (F): Adhesive Component>

-   M6CA: 4-(6-methacryloxyhexyl-1-oxy)cinnamic acid

<Solvent>

Each of the retardation material-forming resin compositions of Examplesand

Comparative Examples contains a solvent. As this solvent, propyleneglycol monomethyl ether (PM) and isopropanol (IPA) were used.

<Measurement of Molecular Weight of Polymer>

The molecular weight of an acrylic copolymer in Polymerization Exampleswas measured with a Shodex (registered trademark) room-temperature gelpermeation chromatography (GPC) apparatus (GPC-101) and a Shodex column(KD-803 and KD-805) as described below.

The number-average molecular weight (hereinafter, called Mn) and theweight-average molecular weight (hereinafter, called Mw) below wereexpressed as values in terms of polystyrene.

Column temperature: 50° C.

Eluant: N,N-dimethylformamide (30 mmol/L of lithium bromide-hydrate(LiBr.H₂O), 30 mmol/L of phosphoric acid⋅anhydride crystal (o-phosphoricacid), and 10 mL/L of tetrahydrofuran (THF) as additives)

Flow rate: 1.0 mL/min

Standard samples for preparing calibration curves: TSK standardpolyethylene oxide (molecular weight: about 900,000, 150,000, 100,000,and 30,000) manufactured by Tosoh Corporation, and polyethylene glycol(molecular weight: about 12,000, 4,000, and 1,000) manufactured byPolymer Laboratories Ltd.

<Measurement of ¹H-NMR>

The analysis device and analysis conditions used for ¹H-NMR analysis areas follows.

Nuclear magnetic resonance apparatus: Varian NMR System 400 NB (400 MHz)

Measurement solvent: CDCl₃

Reference material: tetramethylsilane (TMS) (δ0.0 ppm for ¹H)

Polymerization Example 1

4.0 g of M6CA, 4.0 g of MMA, 2.0 g of HEMA, and 0.3 g of AIBN as apolymerization catalyst were dissolved in 41.2 g of PM, and theresultant solution was caused to react at 80° C. for 20 hours to obtainan acrylic copolymer solution (solid-content concentration: 20% by mass)(P1). Mn and Mw of the obtained acrylic copolymer were 9,300 and 29,000,respectively.

Polymerization Example 2

9.0 g of M6CA, 1.0 g of HEMA, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 41.2 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P2). Mn and Mw ofthe obtained acrylic copolymer were 14,000 and 33,000, respectively.

Polymerization Example 3

7.0 g of M6CA, 10 g of HEMA, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 41.2 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P3). Mn and Mw ofthe obtained acrylic copolymer were 12,000 and 26,200, respectively.

Polymerization Example 4

3.0 g of M6CA, 7.0 g of HEMA, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 41.2 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P4). Mn and Mw ofthe obtained acrylic copolymer were 14,100 and 28,600, respectively.

Polymerization Example 5

5.0 g of M3CA, 5.0 g of HEMA, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 41.2 g of PM, and the resultant solution wascaused to react 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P5). Mn and Mw ofthe obtained acrylic copolymer were 10,800 and 34,900, respectively.

Polymerization Example 6

7.0 g of M6CA, 3.0 g of Karenz MOI-BM, and 0.3 g of AIBN as apolymerization catalyst were dissolved in 41.2 g of PM, and theresultant solution was caused to react at 80° C. for 20 hours to obtainan acrylic copolymer solution (solid-content concentration: 20% by mass)(P6). Mn and Mw of the obtained acrylic copolymer were 13,000 and43,000, respectively.

Polymerization Example 7

7.0 g of M6CAm, 3.0 g of HEMA, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 41.2 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P7). Mn and Mw ofthe obtained acrylic copolymer were 12,000 and 37,000, respectively.

Polymerization Example 8

7.0 g of MMA, 7.0 g of HEMA, 3.5 g of MAA, and 0.5 g of AIBN as apolymerization catalyst were dissolved in 53.9 g of PM, and theresultant solution was caused to react at 70° C. for 20 hours to obtainan acrylic copolymer solution (solid-content concentration: 25% by mass)(P8). Mn and Mw of the obtained acrylic copolymer were 10,300 and24,600, respectively.

Polymerization Example 9

100.0 g of BMAA and 4.2 g of AIBN as a polymerization catalyst weredissolved in 193.5 g of PM, and the resultant solution was caused toreact at 90° C. for 20 hours to obtain an acrylic polymer solution(solid-content concentration: 35% by mass) (P9). Mn and Mw of theobtained acrylic copolymer were 2,700 and 3,900, respectively.

Polymerization Example 10

5.0 g of M6CA, 5.0 g of MMA, and 0.5 g of AIBN as a polymerizationcatalyst were dissolved in 42.0 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P10). Mn and Mw ofthe obtained acrylic copolymer were 7,300 and 16,200, respectively.

Polymerization Example 11

4.0 g of M6CA, 4.0 g of St, 2.0 g of HEMA, and 0.1 g of AIBN as apolymerization catalyst were dissolved in 90.9 g of PM, and theresultant solution was caused to react at 80° C. for 20 hours to obtainan acrylic copolymer solution (solid-content concentration: 10% by mass)(P11). Mn and Mw of the obtained acrylic copolymer were 17,100 and55,300, respectively.

Polymerization Example 12

9.0 g of MMA, 1.0 g of HEMA, and 0.1 g of AIBN as a polymerizationcatalyst were dissolved in 40.4 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P12). Mn and Mw ofthe obtained acrylic copolymer were 15,900 and 29,900, respectively.

Polymerization Example 13

6.0 g of M6CA, 4.0 g of EGAMA, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 41.2 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P13). Mn and Mw ofthe obtained acrylic copolymer were 9,900 and 21,500, respectively.

Polymerization Example 14

7.0 g of M6CAm, 3.0 g of M100, and 0.3 g of AIBN as a polymerizationcatalyst were dissolved in 92.7 g of PM, and the resultant solution wascaused to react at 80° C. for 20 hours to obtain an acrylic copolymersolution (solid-content concentration: 20% by mass) (P14). Mn and Mw ofthe obtained acrylic copolymer were 13,200 and 27,000, respectively.

<Synthesis of Compound (E)>

Synthesis Example 1 Synthesis of Compound [DM-1]

In a nitrogen gas stream, 500 g of ethyl acetate, 35, 5 g (0.300 mol) of1,6-hexanediol, 1.80 g (11.8 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecono(DBU), and 0.45 g (2.04 mmol) of 2,6-di-tert-butyl-para-cresol (BHT)were put in a 2-L four-necked flask at room temperature. This mixturewas heated up to 55° C. with stirring by a magnetic stirrer. Into thisreaction solution, 95.9 g (0.679 mol) of 2-isocyanatoethyl acrylate wasadded dropwise. After being stirred for 2 hours, the reaction solutionwas analyzed by a high performance liquid chromatography. When theintermediate decreased to 1% or less in area percentage, the reactionwas completed. 328 g of hexane was added into the resulting solution,and this mixture was cooled down to the room temperature. Subsequently,the precipitated solid was washed twice with 229 g of hexane and dried,and thus the compound [A-a] was obtained (104 g, 0.260 mol, yield86.7%).

In a nitrogen gas stream, 1,330 g of dichloromethane, 100 g (0.250 mol)of the compound [A-a], and 22.5 g (0.749 mol) of paraformaldehyde wereput in a 2-L four-necked flask. Into this mixture in an ice bath, 122 g(1.12 mol) of trimethylsilyl chloride was added dropwise. After theresulting solution was stirred for 2 hours, a mixed solution of 63.2 g(0.625 mol) of triethylamine and 240 g of methanol was added dropwisetherein. The resulting solution was stirred for 30 minutes, and was thenput in 5-L separatory funnel. 1,500 g of water was added therein, andliquid separation was performed. The obtained organic phase was driedwith magnesium sulfate, filtrate obtained by removing the magnesiumsulfate by filtration was concentrated and dried, and thus the compound[DM-1] was obtained (110 g, 0.226 mol, yield 90.3%). The structure ofthe compound [DM-1] was identified by the spectral data below obtainedby ¹H-NMR analysis.

¹H-NMR (CDCl₃): δ 6.42 (d, 2H J=17.2) 6.17-6.08 (m, 2W), 5.86 (d, 2HJ=10.0), 4.77 (d, 4H J=19.6), 4.30 (m, 4H), 4.12 (t, 4H J=6,4), 3.61 (m,4H), 3.30 (d, 6H J=12.8), 1.67 (m, 4H, 1.40 (m, 4H)

Synthesis Example 2 Synthesis of Compound [DM-2]

In a nitrogen as stream, 35.0 g of ethyl acetate, 87.0 g of toluene,8.41 g (50.0 mmol) of hexamethylene diisocyanate, 0.345 g (2.27 mmol) of1,8-diazabicyclo[5.4.0]-7-undecene (DBU), and 70.0 mg (0.318 mmol) of2,6-di-tert-butyl-para-cresol (BHT) were put in a 500-mL four-neckedflask at room temperature. This mixture was heated up to 60° C. withstirring by a magnetic stirrer. Into this reaction solution, a mixedsolution of 12.8 g (111 mmol) of 2-hydroxyethyl acrylate and 26.0 g oftoluene was added dropwise. The resulting solution was stirred for 1hour, and was then stirred at room temperature for 24 hours. 131 g ofhexane was, added into the resulting solution, and this mixture wascooled in an ice bath. Subsequently precipitated crystals were filteredand dried, and thus the compound [A-b] was obtained (15.0 g, 37.4 mmol,yield 74.8%).

In a nitrogen gas stream, 200 g of dichloromethane, 14.6 g (36.4 mmol)of the compound [A-b], and 3.28 g (109 mmol) of paraformaldehyde wereput in a 300-mL four-necked flask. Into this mixture in an ice bath,23.7 g (218 mmol) of trimethylsilyl chloride was added dropwise. Afterthe resulting solution was stirred for 1 hour, 35.6 g of methanol wasadded dropwise therein and the solution was stirred for 1 hour. Theorganic phase was washed with 300 mL of saturated sodiumhydrogencarbonate aqueous solution, and the obtained aqueous phase wasfurther washed with 200 g of dichloromethane. A solution in which thesetwo organic phases were mixed was further washed with 170 g of brine,and the organic phase obtained was dried with magnesium sulfate. Themagnesium sulfate was removed by filtration, the dichloromethanesolution obtained was concentrated and dried, and thus the [DM-2] as atarget was obtained (16.2 g, 33.1 mmol, yield 91.0%). The structure ofthe compound [DM-2] was identified by the spectral data below obtainedby ¹H-NMR analysis.

¹H-NMR (CDCl₃): δ 6.33 (d, 2H J=17.2), 6.20-6.14 (m, 2H), 5.96 (d, 2HJ=10.4), 4.63 (s, 4H), 4.33 (m, 4H), 4.27 (m, 4H), 3.16-3.14 (br, 10H)1.47 (m, 4H), 1.20 (m, 4H)

<Examples 1 to 22> and <Comparative Examples 1 to 4>

Each of retardation material-forming resin compositions of Examples 1 to22 and Comparative Examples 1 to 4 was prepared according to thecompositions given in Table 1. Subsequently, each of the retardationmaterial-forming resin compositions was used to form a cured film, andthe alignment properties of each cured film obtained were evaluated.

TABLE 1 Component Component Component Component Component Component (B)(C) (D) (D-2) (D-3) Component Component (A) Cross- Containing Cross-Cross- Cross- (E) (F) Alignment Linking Organic Linking Linking LinkingAdhesive Adhesive Polymer Agent Group A Catalyst Catalyst CatalystComponent Component Solvent (g) (g) (g) (g) (g) (g) (g) (g) (g) Example1 P1 HMM PTSA PGME 1.87 0.11 0.015 8.01 Example 2 P1 HMM PTSA PGME 2.120.06 0.013 7.81 Example 3 P2 HMM PTSA PGME 1.87 0.11 0.015 8.01 Example4 P3 HMM PTSA PGME 1.87 0.11 0.015 8.01 Example 5 P4 HMM PTSA PGME 1.870.11 0.015 8.01 Example 6 P1 P9 PTSA PGME 1.87 0.32 0.015 7.80 Example 7P1 HMM P8 PTSA PGME 1.05 0.06 0.84 0.015 8.02 Example 8 P5 HMM PTSA PGME1.87 0.11 0.015 8.01 Example 9 P6 PGME 2.50 7.50 Example 10 P7 HMM PTSAPGME 1.87 0.11 0.015 8.01 Example 11 P1 HMM PTSA BMAA PGME 1.61 0.100.016 0.06 8.21 Example 12 P1 HMM PTSA 80MFA PGME 1.43 0.14 0.014 0.068.36 Example 13 P6 P8 PGME 2.08 0.33 7.58 Example 14 P1 HMM P8 PTSA BMAAPGME 1.28 0.13 0.20 0.015 0.05 8.33 Example 15 P1 P9 P8 PTSA BMAA M6CAPGME 1.10 0.25 0.35 0.018 0.04 0.04 8.20 Example 16 P10 HMM PTSA PGME1.87 0.11 0.015 8.01 Example 17 P11 P9 P12 PTSA DM-1 PGME 2.11 0.31 0.210.015 0.13 7.19 Example 18 P11 P9 P12 PTSA DM-2 PGME 2.11 0.31 0.210.015 0.13 7.19 Example 19 P13 HMM PTSA PGME 1.87 0.11 0.015 8.01Example 20 P13 TC-401 PGME/ 1.92 0.18 IPA 7.87/ 0.03 Example 21 P14 TPDATPS PGME 3.33 0.030 0.130 6.50 Example 22 P14 TAF-2689 PGME 4.85 0.0155.13 Comparative P2 PGME Example 1 2.50 7.50 Comparative P3 PGME Example2 2.50 7.50 Comparative P7 PGME Example 3 2.50 7.50 Comparative P10 PGMEExample 4 2.50 7.50

[Evaluation of Alignment Properties]

A non-alkali glass was spin coated with each of the retardationmaterial-forming resin compositions of Examples and Comparative Examplesby a spin coater at 2000 rpm for 30 seconds, and then the resultant filmwas heated and dried on a hot plate at a temperature of 100° C. for 60seconds to form a cured film. This cured film was vertically irradiatedwith linear polarized light of 313 nm at an exposure amount of 10mJ/cm². A polymerizable liquid crystal solution RMS03-013C forhorizontal alignment manufactured by Merck Ltd., Japan was applied ontothe substrate thus irradiated by a spin coater, and then the resultantcoating was prebaked on a hot plate at 60° C. for 60 seconds to form acoating film having a film thickness of 1.0 μm. This film was exposed at300 mJ/cm² to prepare a retardation material. The retardation materialon the prepared substrate was sandwiched between a pair of polarizingplates, and the emergence of retardation properties in the retardationmaterial was observed. “◯” for those in which retardation propertieswere found without failure, “Δ” for those in which retardationproperties were found with failure, and “×” for those in whichretardation properties were not found are listed in the column “DryingCondition 1”. Those in which the results were “Δ” of “×” were heated anddried under heating and drying conditions for each of the retardationmaterial-forming resin compositions at 100° C. for 60 seconds and thenon a hot plate at 150° C. for 300 seconds, and the same evaluation as inthe “Drying condition 1” was performed. The results are listed in thecolumn “Drying Condition 2”. Those in which the results were “Δ” or “×”in the “Drying Condition 2” were heated and dried under heating anddrying conditions for each of the retardation material-forming resincompositions at 100° C. for 60 seconds and then on a hot plate at 200°C. for 300 seconds, and the same evaluation as in the “Drying condition1” was performed. The results are listed in the column “Drying Condition3”.

[Evaluation Results]

The results of the evaluation performed are given in Table 2.

TABLE 2 Alignment Properties (10 mJ/cm²) Drying Drying Drying Condition1 Condition 2 Condition 3 Example 1 ◯ Example 2 ◯ Example 3 ◯ Example 4◯ Example 5 ◯ Example 6 ◯ Example 7 ◯ Example 8 ◯ Example 9 X X ◯Example 10 Δ ◯ Example 11 ◯ Example 12 ◯ Example 13 X X ◯ Example 14 ◯Example 15 ◯ Example 16 ◯ Example 17 ◯ Example 18 ◯ Example 19 ◯ Example20 ◯ Example 21 X ◯ Example 22 X ◯ Comparative X X X Example 1Comparative X X X Example 2 Comparative X X X Example 3 Comparative X XX Example 4

In Examples 1 to 22, retardation materials were formed at a low exposureamount of 10 mJ/cm² by drying under a preferable drying condition. InComparative Examples 1 to 4 in which the coating films did not havethermosetting properties, liquid crystal alignment properties were notobtained in any drying conditions, and liquid crystal alignmentproperties were not obtained even when the exposure amount was increasedto 30 mJ/cm².

As described above, the retardation material-forming resin compositionof the present invention is used to form a thermally cured film havingphoto-alignment properties, and contains a component having aphoto-alignment moiety and a moiety for thermal cross-linking. Aphoto-aligning group is characterized by being a specific photo-aligninggroup, that is, a photo-aligning group to which a thermally reactivemoiety is bonded directly or connected via a linking group. As for thespecific photo-aligning group, for example, when the photo-aligninggroup is a cinnamic acid residue, the cinnamic acid residue has carboxygroup that is a cross-linking group as a part of the residue. When athermally cross-linking group forms a part of a photoreactive group inthis manner also, the photoreactive group can be included in thespecific photo-aligning group in the composition of the presentinvention.

In the present invention, any component in the composition needs tohave, as the moiety for thermal cross-linking, both of a group Aselected from the group consisting of hydroxy group, carboxy group,amide group, amino group, an alkoxysilyl group, and a group of Formula(2) and a group that reacts with the group A, or any component in thecomposition needs to have a moiety that self-crosslinks by heat.

Thus, the composition of the present invention contains a resin havingthe specific photo-aligning group as the component (A), that is, aphoto-aligning group to which a thermally reactive moiety is bondeddirectly or connected via a linking group.

As one aspect of the present invention, examples include a compositionthat contains the resin having the specific photo-aligning, group as thecomponent (A) and, as the component (B), a cross-linking agent thatreacts with the thermally reactive moiety connected to the specificphoto-aligning group. In this case, the resin of the component (A) onlyneeds to have, as a thermally reactive moiety, the thermally reactivemoiety in the specific photo-aligning group, and this examplecorresponds to Example 16 that contains a copolymer of M6CA with MMA anda cross-linking agent.

As one aspect of the present invention, examples include a compositionthat further contains, as a thermally cross-linking system, a group thatreacts with the thermally reactive moiety connected to the specificphoto-aligning group in the resin of the component (A). This examplecorresponds to Examples 9 to 13, and Example 13 is an example furthercontaining a copolymer having the group A.

A composition in which the resin of the component (A) is a copolymerwith a monomer having the group A, and that contains, as the component(B), a cross-linking agent that thermally reacts with the group A isalso preferred. This example corresponds to Examples 1 to 8, 10 to 12,14, 15, and 17 to 20. Among them, Examples 7, 14, 15, 17, and 18 areexamples further containing a copolymer having the group A, and Examples11, 12, 14, 15, 17, and 18 are examples further having anadhesion-enhancing component.

As one aspect of the present invention, examples include a compositionthat further contains a self-crosslinking group as a thermallycross-linking system in the resin of the component (A). This examplecorresponds to Examples 21 and 22.

INDUSTRIAL APPLICABILITY

The retardation material-forming resin composition according to thepresent invention is very useful as a liquid crystal alignment film fora liquid crystal display element or an orientation material for formingan optically anisotropic film that is provided inside or outside theliquid crystal display element, and is particularly suitable as amaterial for forming a patterned retardation material for a 3D display.Furthermore, the retardation material-forming resin composition issuitable as a material for forming a cured film such as a protectivefilm, a planarization film, and an insulation film in various displayssuch as a thin film transistor (TFT) liquid crystal display element andan organic EL element, particularly as a material for forming aninterlayer insulation film of a TFT liquid crystal element, a protectivefilm for a color filter, an insulation film of an organic EL element, orthe like.

The invention claimed is:
 1. A retardation material-forming resincomposition being thermally curable and comprising a resin, component(A), having a photo-aligning group to which a thermally reactive moietyis bonded directly or connected via a linking group, wherein thephoto-aligning group is an organic group including a structure ofFormula (1):

where R is an OH group; and X¹ is a phenylene group that is optionallysubstituted with an optional substituent.
 2. The retardationmaterial-forming resin composition according to claim 1, wherein theresin of the component (A) is an acrylic copolymer.
 3. The retardationmaterial-forming resin composition according to claim 1, wherein theresin of the component (A) further has a self-crosslinking group, orfurther has a group that reacts with at least one group A selected fromthe group consisting of a hydroxy group, a carboxy group, an amidegroup, an amino group, an alkoxysilyl group, and a group of Formula (2),and when an end portion of the photo-aligning group in the resin is acarboxy group or an amide group, this end portion is also included inthe group A, the group of Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 4. Theretardation material-forming resin composition according to claim 1,wherein the resin of the component (A) further has at least one group Aselected from the group consisting of a hydroxy group, a carboxy group,an amide group, an amino group, an alkoxysilyl group, and a group ofFormula (2), and when an end portion of the photo-aligning group in theresin is a carboxy group or an amide group, this end portion is alsoincluded in the group A, and the composition further includes across-linking agent that reacts with the at least one group A, the groupof Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 5. Theretardation material-forming resin composition according to claim 1,wherein the resin of the component (A) further has a group that reactswith at least one group A selected from the group consisting of ahydroxy group, a carboxy group, an amide group, an amino group, analkoxysilyl group, and a group of Formula (2), and when an end portionof the photo-aligning group in the resin is a carboxy group or an amidegroup, this end portion is also included in the group A, and the groupof Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 6. Theretardation material-forming resin composition according to claim 1,further comprising a compound having at least two groups A selected fromthe group consisting of a hydroxy group, a carboxy group, an amidegroup, an amino group, an alkoxysilyl group, and a group of Formula (2),the group of Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 7. Theretardation material-forming resin composition according to claim 1,further comprising a cross-linking catalyst.
 8. The retardationmaterial-forming resin composition according to claim 1, furthercomprising: a compound having one or more polymerizable groups and atleast one group A selected from the group consisting of a hydroxy group,a carboxy group, an amide group, an amino group, an alkoxysilyl group,and a group of Formula (2), or one or more groups that react with the atleast one group A, the group of Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 9. Theretardation material-forming resin composition according to claim 1,further comprising a monomer having the photo-aligning group to which athermally reactive moiety is bonded directly or connected via a linkinggroup and one or more polymerizable groups.
 10. An orientation materialbeing obtained with the retardation material-forming resin compositionas claimed in claim
 1. 11. A retardation material being formed of acured film that is obtained from the retardation material-forming resincomposition as claimed in claim
 1. 12. A thermally cured-film formationcomposition comprising a resin, component (A), having a photo-aligninggroup to which, a thermally reactive moiety is bonded directly orconnected via a linking group, wherein the photo-aligning group is anorganic group including a structure of Formula (1):

where R is an OH group; and X¹ is a phenylene group that is optionallysubstituted with an optional substituent.
 13. The thermally cured-filmformation composition according to claim 12, wherein the resin of thecomponent (A) is an acrylic copolymer.
 14. The thermally cured-filmformation composition according to claim 12, wherein the resin of thecomponent (A) further has a self-crosslinking group, or further has agroup that reacts with at least one group A selected from the groupconsisting of a hydroxy group, a carboxy group, an amide group, an aminogroup, an alkoxysilyl group, and a group of Formula (2) and when an endportion of the photo-aligning group in the resin is a carboxy group oran amide group, this end portion is also included in the group A, thegroup of Formula (2) having the structure:

where in the Formula, R₅ is an alkyl group, an alkoxy group, or a phenylgroup.
 15. The thermally cured-film formation composition according toclaim 12, wherein the resin of the component (A) further has at leastone of group A selected from the group consisting of a hydroxy group, acarboxy group, an amide group, an amino group, an alkoxysilyl group, anda group of Formula (2), and when an end portion of the photo-aligninggroup in the resin is a carboxy group or an amide group, this endportion is also included in the group A, and the composition furtherincludes a cross-linking agent that reacts with the at least, one groupA, the group of Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 16. Thethermally cured-film formation composition according to claim 12,wherein the resin of the component (A) further has a group that reactswith at least one group A selected from the group consisting of ahydroxy group, a carboxy group, an amide group, an amino group, analkoxysilyl group, and a group of Formula (2), and when an end portionof the photo-aligning group in the resin is a carboxy group or an amidegroup, this end portion is also included in the group A, the group ofFormula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 17. Thethermally cured-film formation composition according to claim 12,further comprising a compound having at least two groups A selected fromthe group consisting of a hydroxy group, a carboxy group, an amidegroup, an amino group, an alkoxysilyl group, and a group of Formula (2),the group of Formula (2) having the structure:

where R₅ is an alkyl group, an alkoxy group, or a phenyl group.
 18. Acured film being obtained with the thermally cured-film formationcomposition as claimed in claim 12.